July 5, 2022

Human Cftr Elisa Kit On Cell Surface

Lab Reagents

Human Elisa Laboratories manufactures the human cftr elisa kit on cell surface reagents distributed by Genprice. The Human Cftr Elisa Kit On Cell Surface reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Human elisa. Other Human products are available in stock. Specificity: Human Category: Cftr Group: Elisa Kit

Elisa Kit information

Human Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) ELISA Kit

RDR-CFTR-Hu-48Tests 48 Tests
EUR 544

Human Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) ELISA Kit

RDR-CFTR-Hu-96Tests 96 Tests
EUR 756

Cftr/ Rat Cftr ELISA Kit

ELI-50883r 96 Tests
EUR 886

QuickTiter Hepatitis B Surface Antigen (HBsAg) ELISA Kit

VPK-5004 96 assays
EUR 914
Description: The QuickTiter Hepatitis B Surface Antigen ELISA Kit measures HBsAg with sensitivity as low as 1 ng/mL. Reagents are sufficient for 96 wells including standards and unknown samples.

QuickTiter Hepatitis B Surface Antigen (HBsAg) ELISA Kit

VPK-5004-5 5 x 96 assays
EUR 3756
Description: The QuickTiter Hepatitis B Surface Antigen ELISA Kit measures HBsAg with sensitivity as low as 1 ng/mL. Reagents are sufficient for 5x96 wells including standards and unknown samples.

Human CFTR ELISA Kit

EHC0458 96Tests
EUR 521

Human CFTR ELISA Kit

STJ150459 1 kit
EUR 412
Description: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of CFTR in human serum, plasma and other biological fluids

CFTR ELISA KIT|Human

EF006688 96 Tests
EUR 689

Human CFTR ELISA KIT

ELI-11169h 96 Tests
EUR 824

ON/ Rat ON ELISA Kit

ELA-E0791r 96 Tests
EUR 886

CFTR ELISA Kit (Human) (OKDD00186)

OKDD00186 96 Wells
EUR 975
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily that is involved in multi-drug resistance. The encoded protein functions as a chloride channel and controls the regulation of other transport pathways. Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens. Alternatively spliced transcript variants have been described, many of which result from mutations in this gene.;Species reactivity: Human;Application: ;Assay info: Quantitative Sandwich ELISA;Sensitivity: < 0.053 ng/mL

CFTR ELISA Kit (Human) (OKCD08127)

OKCD08127 96 Wells
EUR 975
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.059ng/mL

CFTR ELISA Kit (Human) (OKAN06120)

OKAN06120 96 Wells
EUR 792
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.059 ng/mL

Human ON ELISA Kit

EHO0024 96Tests
EUR 521

ON ELISA KIT|Human

EF007025 96 Tests
EUR 689

T-cell surface glycoprotein CD4 ELISA Kit| Sheep T-cell surface

EF019547 96 Tests
EUR 689

Sheep CFTR ELISA Kit

ESC0458 96Tests
EUR 521