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Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) ELISA Kits

CFTR encodes a member of the ATP-binding cassette (ABC) transporter superfamily. Additionally we are shipping CFTR Antibodies (218) and CFTR Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CFTR 12638 P26361
CFTR 24255 P34158
CFTR 1080 P13569
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Top CFTR ELISA Kits at antibodies-online.com

Showing 10 out of 33 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 7 pg/mL 28-1800 pg/mL Typical standard curve 96 Tests Log in to see 11 to 13 Days
$910.56
Details
Dog 4.69 pg/mL 18.75-1200 pg/mL Typical standard curve 96 Tests Log in to see 11 to 13 Days
$1,026.67
Details
Rat 0.1 ng/mL 0.5-10 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Mouse 0.1 ng/mL 0.5-10 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Guinea Pig 0.1 ng/mL 0.5-10 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Rabbit 0.1 ng/mL 0.5-10 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Chicken 0.094 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Pig 0.094 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Monkey 0.1 ng/mL 0.5-10 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Sheep
  96 Tests Log in to see 11 to 13 Days
$707.14
Details

More ELISA Kits for CFTR Interaction Partners

Xenopus laevis Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. NDPK-A (show NME1 ELISA Kits) exists in a functional cellular complex with AMPK (show PRKAA2 ELISA Kits) and CFTR in airway epithelia, and NDPK-A (show NME1 ELISA Kits) catalytic function is required for the AMPK (show PRKAA2 ELISA Kits)-dependent regulation of CFTR

  2. Study conclude that when both CFTR and NPT2a (show SLC34A1 ELISA Kits) are expressed in X. laevis oocytes, CFTR confers to NPT2a (show SLC34A1 ELISA Kits) a cAMPi-dependent trafficking to the membrane.

  3. wild-type CFTR channel gating cycle is essentially irreversible and tightly coupled to the ATPase (show DNAH8 ELISA Kits) cycle, and that this coupling is completely destroyed by the NBD2 Walker B mutation D1370N but only partially disrupted by the NBD1 Walker A mutation K464A.

  4. The cystic fibrosis transmembrane conductance regulator (CFTR) is a protein that belongs to the superfamily of ATP binding cassette (ABC (show ABCB6 ELISA Kits)) transporters.

  5. These data suggest that the Xenopus P2Y1 receptor (show P2RY1 ELISA Kits) can increase both cyclic AMP (show TMPRSS5 ELISA Kits)/protein kinase A and calcium/protein kinase C (show PKC ELISA Kits) levels and that the PKC (show PKC ELISA Kits) pathway is involved in CFTR activation via potentiation of the PKA pathway.

Mouse (Murine) Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. Biotinylation and streptavidin pull-down assays confirmed that CAL dramatically reduces the expression level of total and cell surface Mrp2 in Huh-7 cells. Our findings suggest that CAL interacts with Mrp2 and is a negative regulator of Mrp2 expression.

  2. Myelinosomes secreted from testis somatic TM4 (show TPM4 ELISA Kits) Sertoli cells provide the release of aggregate-prone mutant, but not normal Huntingtin (Htt (show HTT ELISA Kits)) exon1. Myelinosomes also support the release of other aggregate-prone mutant protein responsible for cystic fibrosis (show S100A8 ELISA Kits) (CF), F508delCFTR.

  3. ATP8B1 (show ATP8B1 ELISA Kits) is important for proper CFTR expression and function.

  4. Loss of cystic fibrosis (show S100A8 ELISA Kits) transmembrane regulator impairs intestinal oxalate secretion

  5. CFTR plays a role in suppressing MAPK (show MAPK1 ELISA Kits)/NF-kappaB (show NFKB1 ELISA Kits) to relieve inflammation, reduce proliferation and promote differentiation of keratinocytes, and thus promotes cutaneous wound healing.

  6. physiological fetal hypercalcemia, acting on the CaSR (show CASR ELISA Kits), promotes human fetal lung development via cAMP-dependent opening of CFTR.

  7. CFTR expressed by alveolar or peritoneal macrophages regulates acute proinflammatory responses.

  8. CFTR silencing in pancreatic beta-cells significantly reduced insulin (show INS ELISA Kits) output in response to glucose, and made the cells more sensitive to oxidative stress.

  9. Cftr KO crypt epithelium maintains an alkaline pHi as a consequence of losing both Cl(-) and HCO3 (-) efflux, which impairs pHi regulation by Ae2 (show SLC4A2 ELISA Kits).

  10. Data suggest that the deltaF508 Cftr mutation (the most frequent CFTR mutation in cystic fibrosis (show S100A8 ELISA Kits) in humans) is associated with worsening insulin (show INS ELISA Kits) resistance and down-regulation of insulin (show INS ELISA Kits) secretion from pancreatic beta cells as mutant mice age.

Human Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. RPL12 (show RPL12 ELISA Kits) role in DeltaF508-CFTR protein folding and stability

  2. COOH-terminal sequences mediate enhanced NHERF1 (show SLC9A3R1 ELISA Kits) interaction and facilitate the localization of CFTR.

  3. deltabetagamma-ENaC (show SCNN1A ELISA Kits) is inhibited by CFTR but activated by cyclic AMP (show APRT ELISA Kits).

  4. This study analyzed IL8 (show IL8 ELISA Kits) gene polymorphisms (rs4073, rs2227306 and rs2227307), by means of PCR/RFLP, and their association with pulmonary function markers and clinical severity scores in 186 patients with CF, considering the CFTR genotype.Pulmonary function markers (SaO2 and spirometric variables) and clinical severity scores were also associated with IL8 (show IL8 ELISA Kits) gene polymorphisms.

  5. The cryo-EM structure of human CFTR determined in the dephosphorylated, ATP-free conformation. The structure was analyzed to further establish the architecture of the ion pore, the functions of many positively charged residues, and to identify the structural basis for CFTR's channel activity.

  6. Beta-adrenergically-stimulated sweat rates determined by evaporimetry or by sweat bubble imaging are useful for measuring CFTR function because they provide a near-linear readout across almost the full range of CFTR function

  7. Genes ABCC7, A3, A8, A12 (show UGT1A9 ELISA Kits), and C8 prevailed among the most upregulated or downregulated ones. In conclusion, the results supported our theory about general adenosine triphosphate-binding cassette gene expression profiles and their importance for cancer on clinical as well as research levels.

  8. These studies have demonstrated that Cif (CFTR inhibitory factor), a virulence factor secreted by P. aeruginosa, is associated with reduced lung function in CF and induces the ubiquitination and degradation of wt-CFTR as well as TAP1 (show TAP1 ELISA Kits), which plays a key role in viral and bacterial antigen presentation. [review]

  9. The contribution of EGFR (show EGFR ELISA Kits), EPAC (show RAPGEF3 ELISA Kits), and Ca(2 (show CA2 ELISA Kits)+) in CDCA-induced activation of CFTR-dependent Cl(-) secretion.

  10. The high expression of CFTR in the endometrial carcinoma cells played a pivotal role in restraining the proliferation and transfer of endometrial carcinoma cells.

Pig (Porcine) Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. Results suggest that acetylcholine does not regulate the activity of the CFTR in tracheal epithelia of pigs which opposes observation from studies using mice airway epithelium.

  2. Expression of CFTR-F508del interferes with smooth muscle cell calcium handling and decreases aortic responsiveness.

  3. Pseudomonas aeruginosa and other bacteria into the lumen of intact isolated swine tracheas triggers CFTR-dependent airway surface liquid secretion by the submucosal glands.

  4. TGF-beta1 (show TGFB1 ELISA Kits), via TGF-beta1 (show TGFB1 ELISA Kits) receptor I and p38 MAPK (show MAPK14 ELISA Kits) signaling, reduces CFTR expression to impair CFTR-mediated anion secretion, which would likely compound the effects associated with mild CFTR mutations and ultimately would compromise male fertility.

  5. The esophageal submucosal glands (SMG (show SNRPG ELISA Kits)) secrete HCO(3)(-) and mucus into the esophageal lumen, where they contribute to acid clearance and epithelial protection. We investigated the presence of CFTR, its involvement in the secretion process, and the effect of cAMP on HCO3 secretion in this tissue. This is the first report on the presence of CFTR channels in the esophagus.

  6. data suggest that loss of CFTR directly alters Schwann cell function and that some nervous system defects in people with cystic fibrosis (show S100A8 ELISA Kits) are likely primary

  7. The data suggest, that during bacterial infections and resulting release of proinflammatory cytokines, the glands are stimulated to secrete fluid, and this response is mediated by cAMP-activated CFTR.

  8. CFTR is required for maximal liquid absorption by lung alveoli under cAMP stimulation

  9. These findings reveal differences between nasal and tracheal glands, show defective fluid secretion in nasal glands of cystic fibrosis (show S100A8 ELISA Kits) pigs, reveal some spared function in the DeltaF508 vs. null piglets.

  10. causal link between CFTR mutations and partial or total vas (show AVP ELISA Kits) deferens and/or epididymis atresia at birth

Cow (Bovine) Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. conserved CFTR sequences between species are examined for potential regulatory elements. Regions of introns 2, 3, 10, 17a, 18, and 21 and 3' flanking sequence corresponding to human CFTR DNase I (show DNASE1 ELISA Kits) hypersensitive sites showed high homology in cow and pig.

Guinea Pig Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR) interaction partners

  1. Results demonstrate functional coupling between Cftr and Slc26a6 (show SLC26A6 ELISA Kits)-like Cl(-)/HCO(3)(-) exchange activity in apical membrane of guinea pig pancreatic interlobular duct.

CFTR Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with CFTR

  • cystic fibrosis transmembrane conductance regulator (cftr-A) antibody
  • cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (CFTR) antibody
  • cystic fibrosis transmembrane conductance regulator (Cftr) antibody
  • cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (Cftr) antibody
  • cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (cftr) antibody
  • cystic fibrosis transmembrane conductance regulator homolog (Cftr) antibody
  • abc35 antibody
  • abcc7 antibody
  • AW495489 antibody
  • CF antibody
  • CFTR antibody
  • cftr/mrp antibody
  • dJ760C5.1 antibody
  • mrp7 antibody
  • RGD1561193 antibody
  • tnr-cftr antibody
  • xcftr antibody

Protein level used designations for CFTR

cystic fibrosis transmembrane conductance regulator , cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) , cystic fibrosis transmembrane conductance regulator, ATP-binding cassette (sub-family C, member 7) , ATP-binding cassette sub-family C member 7 , ATP-binding cassette transporter sub-family C member 7 , ATP-binding cassette, subfamily c, member 7 , cAMP-dependent chloride channel , channel conductance-controlling ATPase , cystic fibrosis transmembrane conductance regulator homolog , cystic fibrosis transmembrane conductance regulator homolog; ATP-binding cassette, subfamily c, member 7 , CFTR chloride channel , chloride channel , CFTR cAMP-dependent chloride channel protein , Channel conductance-controlling ATPase

GENE ID SPECIES
373725 Xenopus laevis
780954 Monodelphis domestica
100137161 Nomascus leucogenys
12638 Mus musculus
24255 Rattus norvegicus
1080 Homo sapiens
100049619 Gallus gallus
492302 Canis lupus familiaris
403154 Sus scrofa
281067 Bos taurus
100009471 Oryctolagus cuniculus
100719898 Cavia porcellus
100071259 Equus caballus
443347 Ovis aries
100381094 Xenopus laevis
100137035 Pongo abelii
463674 Pan troglodytes
100126675 Papio anubis
100135647 Cavia porcellus
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