Anticorps Polyclonal de lapin anti-CFTR

CFTR Polyclonal Antibody for IHC, FC (Intra), Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

IHC, FC (Intra), Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 20738-1-PBS

Synonymes

ABCC7, ATP-binding cassette sub-family C member 7, cAMP-dependent chloride channel, CFTR/MRP, Channel conductance-controlling ATPase



Informations sur le produit

20738-1-PBS cible CFTR dans les applications de IHC, FC (Intra), Indirect ELISA et montre une réactivité avec des échantillons Humain

Réactivité Humain
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène Peptide
Nom complet cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
Masse moléculaire calculée 168 kDa
Numéro d’acquisition GenBankNM_000492
Symbole du gène CFTR
Identification du gène (NCBI) 1080
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

      What is the human cytogenetic location of the CFTR gene?

7q31.2

 

What is the predicted molecular weight of CFTR? 

168 kDa

 

Where is CFTR expressed?

CFTR is mainly expressed in apical membranes of vertebrate epithelial cells.

 

What is the ion selectivity of CFTR?

CFTR is an anion-selective channel, responsible for regulating chloride and bicarbonate transport.

 

What is the process of CFTR trafficking?

The ER provides the first steps in CFTR folding quality control. CFTR can be degraded by the ER associated degradation (ERAD) pathway, or it is transported to the Golgi for maturation before being trafficked to the cell membrane.

 

What are the separate domains of CFTR?

CFTR consists of two transmembrane domains, two nucleotide binding domains, and a regulatory domain.

 

What regulates CFTR?

CFTR activity is ATP-dependent and is regulated by protein kinase A phosphorylation.

 

What is the role of CFTR?

CFTR functions as a channel for anions, regulating water and ionic homeostasis.

 

What mutations in CFTR leads to protein degradation?

Deletion of the regulatory domain or the phenylalanine 508 (F508del) results in an increase in CFTR degradation. This degradation then leads to a decrease of secretion product clearance and an increase in viscous mucosal buildup at the epithelial surface of affected organs, the primary symptom of cystic fibrosis. Mutations in CFTR can also lead congenital bilateral absence of vas deferens (CBAVD) or sperm abnormalities in men.

 

How does CFTR differ from other ATP-binding cassette proteins?

Unlike other proteins in the ABC family, CFTR functions as an ion channel.


PMIDs: 24513531, 24534272, 22966013, 22709980


{{ptg:RelatedPrimaryAntibodies}}