RM and Biomed LTD. Physiology Bioresonance Medium,Monoclonal,Recombinant Alhagi maurorum important oil and research of its antimicrobial

Alhagi maurorum important oil and research of its antimicrobial


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rmbiomed

rmbiomed

A Standardized Inverter Package deal Borne by Broad Host Vary Plasmids for Genetic Circuit Design in Gram-Damaging Micro organism

Genetically encoded logic gates, particularly inverters-NOT gates-are the constructing blocks for designing circuits, engineering biosensors, or decision-making gadgets in artificial biology. Nonetheless, the repertoire of inverters available for various species is moderately restricted. On this work, a big complete of NOT gates that was proven to operate beforehand in a particular pressure of Escherichia coli, was recreated as broad host vary (BHR) assortment of constructs assembled in low, medium, and excessive copy quantity plasmid backbones of the SEVA (Normal European Vector Structure) assortment.
The enter/output operate of every of the gates was characterised and parametrized within the environmental bacterium and metabolic engineering chassis Pseudomonas putida. Comparisons of the ensuing fluorescence cytometry information with these printed for a similar gates in Escherichia coli supplied helpful hints on the portability of the corresponding gates.
The hereby described inverter bundle (20 totally different variations of 12 distinct gates) borne by BHR plasmids thus turns into a toolbox of selection for designing genetic circuitries in quite a lot of Gram-negative species apart from E. coli.

Formulation and characterization of nanoemulsion from Alhagi maurorum important oil and research of its antimicrobial, antibiofilm, and plasmid curing exercise in opposition to antibiotic-resistant pathogenic micro organism

Nanoemulsion expertise is an alternate candidate to beat antibiotic resistance in pathogenic micro organism. The intention of this analysis was nanoemulsion manufacturing from the important oil of Alhagi maurorum and the characterization of this nanostructure. Nanoemulsion of important oil from A. maurorum was ready utilizing the ionotropic gelation technique and chitosan as a nano-carrier. Scanning Electron Microscopy (SEM) was used to characterize the synthesized nanoparticles.
The impact of nanoemulsion on the antibacterial, antibiofilm, and plasmid curing of six antibiotic-resistant pathogenic micro organism (P. aeruginosa, E. coli, S. aureus, Okay. pneumonia, A. baumannii, B. cereus) was evaluated.
  • The outcomes of this research confirmed that nanoparticles had a spherical form and easy topology. The imply dimension had been 172 ± four nm and Zeta potentials was +28.6 mv. The outcomes of antibacterial exercise confirmed that nanoemulsion of important oil had larger inhibition in opposition to micro organism in comparison with free important oil.
  • Additionally, this nanoemulsion had antibiofilm exercise. Minimal Inhibitory Focus (MIC) and Minimal Bactericidal Focus for Biofilm (MBCB) had been decided for nanoemulsion in opposition to the biofilm of pathogenic micro organism.
  • The outcomes have proven that the MIC worth for A. baumannii is 12.5 mg ml -1 and for E. coli this worth is 1.75 mg ml -1. This discovering implies that MIC values had been highest for A. baumannii and lowest for E. coli. Statistical evaluation demonstrated that the inhibitory impact of nanoemulsion in opposition to bacterial biofilm was important (P < 0.05).
  • This nanoemulsion additionally had a exceptional impact the curing of R-plasmid of three antibiotic-resistant micro organism. Based on GC-MS evaluation of A. maurorum important oil, the principle compounds had been oxygenated sesquiterpenes and hydrocarbons. Nanoemulsion of A. maurorum had the potential to make use of as appropriate antimicrobial brokers in opposition to antibiotic-resistant micro organism.

Emergence of plasmid-mediated mcr genes from Gram-negative micro organism on the human-animal interface

Background: The worldwide emergence of plasmid-mediated colistin resistance (Col-R) conferred by mcr genes in gram-negative rods (GNRs) has jeopardized the final therapy possibility for multidrug-resistant bacterial infections in people. This research aimed to evaluate the emergence of mcr gene-mediated Col-R in GNRs remoted from people and animals in Pakistan.
Strategies: Animal and medical specimens collected from numerous sources had been prospectively analysed utilizing commonplace microbiological procedures. Pathogens had been recognized utilizing the API 20E and API 20NE methods (bioMerieux).
Minimal inhibitory focus (MIC) in opposition to colistin was decided utilizing the MIC detection strategies, and multiplex polymerase chain response (PCR) was used to amplify the mcr-1 to mcr-5 genes.
Outcomes: We remoted 126 (88.1%) animal and 17 (11.9%) human Col-R phenotypes, amongst which there was a big affiliation (P < 0.01) of Escherichia coli and Proteus mirabilis with animals and of Acinetobacter baumannii with people.
Animal strains exhibited statistically important (P < 0.05) resistance to co-trimoxazole, chloramphenicol, and moxifloxacin, and the human pathogens exhibited statistically important (P < 0.05) antibiotic resistance to cephalosporins, carbapenems, and piperacillin-tazobactam.
For Col-R strains, MIC50 values had been > 6 µg/mL and > 12 µg/mL for human and animal isolates, respectively. mcr genes had been detected in 110 (76.9%) bacterial strains, of which 108 (98.2%) had been mcr-1 and a couple of (1.8%) had been mcr-2.
Conclusions: The detection of a substantial variety of MCR-1 and MCR-2 genes in animals is worrisome, as they’re now being detected in medical pathogens. The acquisition of mcr genes by colistin-susceptible micro organism might go away us in a post-antibiotic period.
Key phrases: Antibacterial profile; Antimicrobial resistance; Colistin resistance; Cell colistin resistance; Plasmid-mediated resistance; mcr genes.

Replication Protein A2 (RPA2) Antibody

20-abx211199
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Replication Protein A1 (RPA1) Antibody

20-abx174378
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  • 1 mg
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Replication Protein A1 (RPA1) Antibody

20-abx174379
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  • 1 mg
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Replication Protein A1 (RPA1) Antibody

20-abx178250
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  • 1 mg
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Replication Protein A1 (RPA1) Antibody

20-abx178251
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Replication Protein A2 (RPA2) Antibody

20-abx125040
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  • 100 ul
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Replication Protein A1 (RPA1) Antibody

abx237391-100ug 100 ug
EUR 610.8

Replication Protein A2 (RPA2) Antibody

abx237392-100ug 100 ug
EUR 610.8

Replication Protein A3 (RPA3) Antibody

abx237393-100ug 100 ug
EUR 661.2

Replication Protein A1 (RPA1) Antibody

abx159678-100ul 100 ul
EUR 560.4

Replication Protein A2 (RPA2) Antibody

abx159679-100ul 100 ul
EUR 560.4

Replication Protein A3 (RPA3) Antibody

20-abx142199
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  • 100 ul
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Replication Protein A3 (RPA3) Antibody

20-abx006386
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Replication Protein A1 (RPA1) Antibody

20-abx007829
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  • 100 ul
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Replication Protein A1 (RPA1) Antibody

abx010302-100ug 100 ug
EUR 493.2

Replication Protein A1 (RPA1) Antibody

20-abx000943
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Replication Protein A2 (RPA2) Antibody

20-abx001801
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Replication Protein A1 (RPA1) Antibody

abx028041-400ul 400 ul
EUR 627.6

Replication Protein A1 (RPA1) Antibody

abx028041-80l 80 µl
EUR 343.2

Rat Replication Protein A1 ELISA Kit

IRTRPA1KT each
EUR 790
Description: Rat Replication Protein A1 ELISA Kit

RPA32 Antibody / Replication Protein A2

RQ5919 100 ug
EUR 356.15
Description: This gene encodes a subunit of the heterotrimeric Replication Protein A (RPA) complex, which binds to single-stranded DNA (ssDNA), forming a nucleoprotein complex that plays an important role in DNA metabolism, being involved in DNA replication, repair, recombination, telomere maintenance, and co-ordinating the cellular response to DNA damage through activation of the ataxia telangiectasia and Rad3-related protein (ATR) kinase. The RPA complex protects single-stranded DNA from nucleases, prevents formation of secondary structures that would interfere with repair, and co-ordinates the recruitment and departure of different genome maintenance factors. The heterotrimeric complex has two different modes of ssDNA binding, a low-affinity and high-affinity mode, determined by which oligonucleotide/oligosaccharide-binding (OB) domains of the complex are utilized, and differing in the length of DNA bound. This subunit contains a single OB domain that participates in high-affinity DNA binding and also contains a winged helix domain at its carboxy terminus, which interacts with many genome maintenance protein. Post-translational modifications of the RPA complex also plays a role in co-ordinating different damage response pathways.

RPA32 Antibody / Replication Protein A2

V7886-100UG 100 ug
EUR 349.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7886-20UG 20 ug
EUR 153.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7886SAF-100UG 100 ug
EUR 349.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V8066-100UG 100 ug
EUR 424.15
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V8066-20UG 20 ug
EUR 186.15
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V8066SAF-100UG 100 ug
EUR 424.15
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7341-100UG 100 ug
EUR 349.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7341-20UG 20 ug
EUR 153.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7341IHC-7ML 7 ml
EUR 424.15
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7341SAF-100UG 100 ug
EUR 349.3
Description: Recognizes a protein of 34kDa, identified as a subunit of Replication Protein A (RPA) (also known as human single-stranded DNA binding protein, or HSSB). RPA from human cells is a stable heterotrimer of 70kDa, 32-34kDa, and 11-14kDa subunits (RPA70, RPA32, and RPA14 respectively). It is involved in DNA replication, repair, and recombination. RPA is required for the SV40 large tumor antigen-catalyzed unwinding of SV40 DNA and stimulates DNA polymerase (pol) alpha and delta. RPA34 is phosphorylated at the G1/S boundary of the cell cycle or upon exposure of cells to DNA damage-inducing agents including ionizing and UV radiation.

RPA32 Antibody / Replication Protein A2

V7392-100UG 100 ug
EUR 424.15
Description: As part of the heterotrimeric replication protein A complex (RPA/RP-A), binds and stabilizes single-stranded DNA intermediates, that form during DNA replication or upon DNA stress. It prevents their reannealing and in parallel, recruits and activates different proteins and complexes involved in DNA metabolism. Thereby, it plays an essential role both in DNA replication and the cellular response to DNA damage. In the cellular response to DNA damage, the RPA complex controls DNA repair and DNA damage checkpoint activation. Through recruitment of ATRIP activates the ATR kinase a master regulator of the DNA damage response. It is required for the recruitment of the DNA double-strand break repair factors RAD51 and RAD52 to chromatin in response to DNA damage. Also recruits to sites of DNA damage proteins like XPA and XPG that are involved in nucleotide excision repair and is required for this mechanism of DNA repair. Plays also a role in base excision repair (BER) probably through interaction with UNG. Also recruits SMARCAL1/HARP, which is involved in replication fork restart, to sites of DNA damage. May also play a role in telomere maintenance. [UniProt]

RPA32 Antibody / Replication Protein A2

V7392-20UG 20 ug
EUR 186.15
Description: As part of the heterotrimeric replication protein A complex (RPA/RP-A), binds and stabilizes single-stranded DNA intermediates, that form during DNA replication or upon DNA stress. It prevents their reannealing and in parallel, recruits and activates different proteins and complexes involved in DNA metabolism. Thereby, it plays an essential role both in DNA replication and the cellular response to DNA damage. In the cellular response to DNA damage, the RPA complex controls DNA repair and DNA damage checkpoint activation. Through recruitment of ATRIP activates the ATR kinase a master regulator of the DNA damage response. It is required for the recruitment of the DNA double-strand break repair factors RAD51 and RAD52 to chromatin in response to DNA damage. Also recruits to sites of DNA damage proteins like XPA and XPG that are involved in nucleotide excision repair and is required for this mechanism of DNA repair. Plays also a role in base excision repair (BER) probably through interaction with UNG. Also recruits SMARCAL1/HARP, which is involved in replication fork restart, to sites of DNA damage. May also play a role in telomere maintenance. [UniProt]

RPA32 Antibody / Replication Protein A2

V7392SAF-100UG 100 ug
EUR 424.15
Description: As part of the heterotrimeric replication protein A complex (RPA/RP-A), binds and stabilizes single-stranded DNA intermediates, that form during DNA replication or upon DNA stress. It prevents their reannealing and in parallel, recruits and activates different proteins and complexes involved in DNA metabolism. Thereby, it plays an essential role both in DNA replication and the cellular response to DNA damage. In the cellular response to DNA damage, the RPA complex controls DNA repair and DNA damage checkpoint activation. Through recruitment of ATRIP activates the ATR kinase a master regulator of the DNA damage response. It is required for the recruitment of the DNA double-strand break repair factors RAD51 and RAD52 to chromatin in response to DNA damage. Also recruits to sites of DNA damage proteins like XPA and XPG that are involved in nucleotide excision repair and is required for this mechanism of DNA repair. Plays also a role in base excision repair (BER) probably through interaction with UNG. Also recruits SMARCAL1/HARP, which is involved in replication fork restart, to sites of DNA damage. May also play a role in telomere maintenance. [UniProt]

Replication Protein A2 (RPA2) ELISA Kit

abx595526-96tests 96 tests
EUR 764.4

Replication Protein A1, 70 kDa Antibody

20-abx115128
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  • 150 ul
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Replication Protein A2, 32 kDa Antibody

20-abx115129
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  • 150 ul
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Replication Protein A4, 34 kDa Antibody

20-abx115130
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  • 150 ul
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Human Replication Protein A1 ELISA Kit

IHURPA1KT each
EUR 733
Description: Human Replication Protein A1 ELISA Kit

Replication Protein A4, 34 kDa Antibody

abx115130-100l 100 µl
EUR 612.5

Recombinant Replication Protein A1 (RPA1)

RPU57621-100ug 100ug
EUR 470.4

Recombinant Replication Protein A1 (RPA1)

RPU57621-1mg 1mg
EUR 2184

Recombinant Replication Protein A1 (RPA1)

RPU57621-50ug 50ug
EUR 385

Recombinant Replication Protein A1 (RPA1)

RPU57622-100ug 100ug
EUR 470.4

Recombinant Replication Protein A1 (RPA1)

RPU57622-1mg 1mg
EUR 2184

Recombinant Replication Protein A1 (RPA1)

RPU57622-50ug 50ug
EUR 385

Recombinant Replication Protein A1 (RPA1)

RPH217Hu01 10ug
EUR 140

Recombinant Replication Protein A1 (RPA1)

RPH217Ra01 10ug
EUR 140

Recombinant Human Replication Protein A2

7-06178 2µg Ask for price

Recombinant Human Replication Protein A2

7-06179 10µg Ask for price

Recombinant Human Replication Protein A2

7-06180 1mg Ask for price

Replication Protein A2 Human Recombinant

rAP-3734 Inquiry Ask for price

Rat Replication Protein A1 (RPA1) CLIA Kit

20-abx495409
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  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests

Replication Protein A1 (RPA1) Antibody (HRP)

20-abx315981
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  • 100 ug
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Rat Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Ra 96T
EUR 499
Description: tissue homogenates, cell lysates or other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Ra-48T 48T
EUR 658.8
Description: A sandwich quantitative ELISA assay kit for detection of Rat Replication Protein A1 (RPA1) in samples from tissue homogenates, cell lysates or other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Ra-96T 96T
EUR 861.6
Description: A sandwich quantitative ELISA assay kit for detection of Rat Replication Protein A1 (RPA1) in samples from tissue homogenates, cell lysates or other biological fluids.

Rat RPA1(Replication Protein A1) ELISA Kit

ELK6959-48T 48T Ask for price
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat RPA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat RPA1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat RPA1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat RPA1 in the samples is then determined by comparing the OD of the samples to the standard curve.

Rat RPA1(Replication Protein A1) ELISA Kit

ELK6959-96T 96T Ask for price
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat RPA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat RPA1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat RPA1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat RPA1 in the samples is then determined by comparing the OD of the samples to the standard curve.

Rat Replication Protein A1 (RPA1) ELISA Kit

EKU07081-48T 48T
EUR 603.26

Rat Replication Protein A1 (RPA1) ELISA Kit

EKU07081-5x96T 5x96T
EUR 4093.55

Rat Replication Protein A1 (RPA1) ELISA Kit

EKU07081-96T 96T
EUR 861.8

Rat Replication Protein A1 (RPA1) ELISA Kit

EKN48192-48T 48T
EUR 410.83

Rat Replication Protein A1 (RPA1) ELISA Kit

EKN48192-5x96T 5x96T
EUR 2787.78

Rat Replication Protein A1 (RPA1) ELISA Kit

EKN48192-96T 96T
EUR 586.9

Rat Replication Protein A1 (RPA1) ELISA Kit

DL-RPA1-Ra 96T
EUR 475
Description: tissue homogenates, cell lysates or other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

EK16449 96Т
EUR 768

Pig Replication Protein A1 (RPA1) ELISA Kit

abx360874-96tests 96 tests
EUR 990

Rat Replication Protein A1 (RPA1) ELISA Kit

20-abx156054
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  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests

Rat Replication Protein A1 (RPA1) ELISA Kit

RD-RPA1-Ra-48T 48T
EUR 487.7
Description: tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

RD-RPA1-Ra-48Tests 48 Tests
EUR 668.4

Rat Replication Protein A1 (RPA1) ELISA Kit

RD-RPA1-Ra-96T 96T
EUR 696.7
Description: tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

RD-RPA1-Ra-96Tests 96 Tests
EUR 930

Rat Replication Protein A1(RPA1) ELISA Kit

NSL0189r 96 Tests
EUR 498

Rat Replication Protein A1 (RPA1) ELISA Kit

RDR-RPA1-Ra-48T 48T
EUR 512.09
Description: tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

RDR-RPA1-Ra-48Tests 48 Tests
EUR 699.6

Rat Replication Protein A1 (RPA1) ELISA Kit

RDR-RPA1-Ra-96T 96T
EUR 731.54
Description: tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

RDR-RPA1-Ra-96Tests 96 Tests
EUR 973.2

ELISA Kit for Replication Protein A1 (RPA1)

SEH217Hu 96Т
EUR 700

ELISA Kit for Replication Protein A1 (RPA1)

SEH217Ra 96Т
EUR 760

Rat Replication Protein A1 (RPA1) ELISA Kit

SEH217Ra-10x96wellstestplate 10x96-wells test plate
EUR 6149.04
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Replication Protein A1 (RPA1) in Tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

SEH217Ra-1x48wellstestplate 1x48-wells test plate
EUR 611.57
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Replication Protein A1 (RPA1) in Tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

SEH217Ra-1x96wellstestplate 1x96-wells test plate
EUR 822.24
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Replication Protein A1 (RPA1) in Tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

SEH217Ra-5x96wellstestplate 5x96-wells test plate
EUR 3340.08
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Replication Protein A1 (RPA1) in Tissue homogenates, cell lysates and other biological fluids.

Rat Replication Protein A1 (RPA1) ELISA Kit

4-SEH217Ra
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  • 10 plates of 96 wells
  • 5 plates of 96 wells
  • 1 plate of 96 wells
Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Rat Replication Protein A1 (RPA1) in samples from Tissue homogenates, cell lysates and other biological fluids. with no significant corss-reactivity with analogues from other species.

Replication Protein A1 (RPA1) Antibody (FITC)

20-abx315982
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  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Replication Protein A2 (RPA2) Antibody Pair

abx117402-1pair5x96wellplates 1 pair (5x96 well plates)
EUR 1212

Replication Protein A2 (RPA2)(RPA2/2106), 0.2mg/mL

BNUB2106-100 1uL
EUR 225
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

Replication Protein A2 (RPA2)(RPA2/2106), 0.2mg/mL

BNUB2106-500 1uL
EUR 485
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

Replication Protein A2 (RPA2)(RPA2/2106), 1mg/mL

BNUM2106-50 1uL
EUR 396
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

RPA32 Antibody / RPA2 / Replication Protein A2

RQ6589 100ug
EUR 356.15
Description: This gene encodes a subunit of the heterotrimeric Replication Protein A (RPA) complex, which binds to single-stranded DNA (ssDNA), forming a nucleoprotein complex that plays an important role in DNA metabolism, being involved in DNA replication, repair, recombination, telomere maintenance, and co-ordinating the cellular response to DNA damage through activation of the ataxia telangiectasia and Rad3-related protein (ATR) kinase. The RPA complex protects single-stranded DNA from nucleases, prevents formation of secondary structures that would interfere with repair, and co-ordinates the recruitment and departure of different genome maintenance factors. The heterotrimeric complex has two different modes of ssDNA binding, a low-affinity and high-affinity mode, determined by which oligonucleotide/oligosaccharide-binding (OB) domains of the complex are utilized, and differing in the length of DNA bound. This subunit contains a single OB domain that participates in high-affinity DNA binding and also contains a winged helix domain at its carboxy terminus, which interacts with many genome maintenance protein. Post-translational modifications of the RPA complex also plays a role in co-ordinating different damage response pathways.

Human Replication Protein A1 (RPA1) CLIA Kit

20-abx495408
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  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests

Goat Replication Protein A1(RPA1) ELISA Kit

NSL0204Gt 96T
EUR 528

Replication Protein A2 (RPA2)(RPA2/3140R), 0.2mg/mL

BNUB3140-100 1uL
EUR 225
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

Replication Protein A2 (RPA2)(RPA2/3140R), 0.2mg/mL

BNUB3140-500 1uL
EUR 485
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

Replication Protein A2 (RPA2)(RPA2/3140R), 1mg/mL

BNUM3140-50 1uL
EUR 396
Description: Primary and secondary antibodies for multiple methodologyimmunostaining detection application

Replication Protein A1 (RPA1) Antibody (Biotin)

20-abx315983
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  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Human Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Hu 96T
EUR 463
Description: tissue homogenates or other biological fluids.

Human Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Hu-48T 48T
EUR 620.4
Description: A sandwich quantitative ELISA assay kit for detection of Human Replication Protein A1 (RPA1) in samples from tissue homogenates or other biological fluids.

Human Replication Protein A1 (RPA1) ELISA Kit

DLR-RPA1-Hu-96T 96T
EUR 807.6
Description: A sandwich quantitative ELISA assay kit for detection of Human Replication Protein A1 (RPA1) in samples from tissue homogenates or other biological fluids.

Human RPA1(Replication Protein A1) ELISA Kit

ELK4413-48T 48T Ask for price
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human RPA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RPA1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human RPA1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human RPA1 in the samples is then determined by comparing the OD of the samples to the standard curve.

Human RPA1(Replication Protein A1) ELISA Kit

ELK4413-96T 96T Ask for price
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human RPA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RPA1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human RPA1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human RPA1 in the samples is then determined by comparing the OD of the samples to the standard curve.

Human Replication Protein A1 (RPA1) ELISA Kit

EKU07080-48T 48T
EUR 555.66

Human Replication Protein A1 (RPA1) ELISA Kit

EKU07080-5x96T 5x96T
EUR 3770.55

Human Replication Protein A1 (RPA1) ELISA Kit

EKU07080-96T 96T
EUR 793.8

Human Replication Protein A1 (RPA1) ELISA Kit

EKN48191-48T 48T
EUR 378.7

Human Replication Protein A1 (RPA1) ELISA Kit

EKN48191-5x96T 5x96T
EUR 2569.75

Human Replication Protein A1 (RPA1) ELISA Kit

EKN48191-96T 96T
EUR 541

Human Replication Protein A1 (RPA1) ELISA Kit

DL-RPA1-Hu 96T
EUR 441
Description: tissue homogenates or other biological fluids.

Human Replication Protein A1 (RPA1) ELISA Kit

EK16448 96Т
EUR 768

Human Replication Protein A1 (RPA1) ELISA Kit

abx573009-96tests 96 tests
EUR 943.2

Human Replication Protein A2 (RPA2) ELISA Kit

abx382883-96tests 96 tests
EUR 1093.2

Human Replication Protein A3 (RPA3) ELISA Kit

abx382884-96tests 96 tests
EUR 1093.2

Human Replication Protein A1 (RPA1) ELISA Kit

20-abx152981
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  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests

Human Replication Protein A1 (RPA1) ELISA Kit

RD-RPA1-Hu-48T 48T
EUR 452.7
Description: tissue homogenates and other biological fluids.

Speedy and easy pressure-sensitive adhesive microdevice fabrication for sequence-specific seize and fluorescence detection of sepsis-related bacterial plasmid gene sequences

Microbial resistance to at the moment out there antibiotics poses an amazing menace within the international combat in opposition to infections. An necessary step in figuring out bacterial antibiotic resistance may be selective DNA sequence seize and fluorescence labeling. On this paper, we show the fabrication of straightforward, strong, cheap microfluidic gadgets for DNA seize and fluorescence detection of a mannequin antibiotic resistance gene sequence.
We laser micromachined polymethyl methacrylate microchannels and enclosed them utilizing pressure-sensitive adhesive tapes.
We then shaped porous polymer monoliths with DNA seize probes in these microchannels and used them for sequence-specific seize, fluorescent labeling, and laser-induced fluorescence detection of picomolar (pM) concentrations of artificial and plasmid antibiotic resistance gene targets.
The relative fluorescence for the elution peaks elevated with loaded goal DNA focus. We noticed larger fluorescence sign and % restoration for artificial goal DNA in comparison with plasmid DNA on the similar loaded goal focus. A non-target gene was used for management experiments and produced < 3% seize relative to the identical focus of the goal.
The total evaluation course of together with system fabrication was accomplished in lower than 90 min with a restrict of detection of 30 pM. The simplicity of system fabrication and good DNA seize selectivity demonstrated herein have the potential for software with processes for bacterial plasmid DNA extraction and single-particle counting to facilitate the willpower of antibiotic susceptibility. Graphical summary.

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