ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR

ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Struktur
CAS-Nr.
Englisch Name:
ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
Synonyma:
ABCC7;ANTI-CFTR;ANTI-ABCC7;ANTI-HUMAN ELT;cAMP- dependent chloride channel;Anti-cAMP-dependent chloride channel;Anti-CFTR antibody produced in rabbit;ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;Anti-ATP-binding cassette transporter sub-family C member 7;ANTI-HUMAN CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
CBNumber:
CB4198590
Summenformel:
Molgewicht:
0
MOL-Datei:
Mol file

ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Eigenschaften

storage temp. 
-20°C
Aggregatzustand
buffered aqueous glycerol solution

Sicherheit

ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project (www.proteinatlas.org)and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. To view these protocols and other useful information about Prestige Antibodies and the HPA, visit .

Allgemeine Beschreibung

CFTR (Cystic fibrosis transmembrane conductance regulator, ATP-binding cassette sub-family C, member 7) is a membrane-associated, N-linked glycoprotein.

Biochem/physiol Actions

CFTR (Cystic fibrosis transmembrane conductance regulator, ATP-binding cassette sub-family C, member 7) is mainly involved in the regulation of Na+ and Cl- transport by acting as a linear, cAMP activated, chloride channel. In addition, it is also associated with different transport signaling pathways. It has been reported that CFTR controls functionality of outwardly rectifying Cl- channels (ORCCs) by facilitating the transport and delivery of potent autacoid agonist and ORCC regulator ATP. It has also been suggested that CFTR can interact with Na+-reabsorptive pathway. CFTR is associated with congenital bilateral absence of the vas deferens (CBAVD) and causes the genital form of cystic fibrosis (CF). The CFTR gene may also responsible for male infertility.

ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 16)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Sigma-Aldrich 021-61415566 800-8193336
orderCN@merckgroup.com China 51471 80
Shanghai guandao biology engineering co., ltd 18818239863 18818239863
3171921642@qq.com China 8889 58

  • ANTI-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
  • ANTI-HUMAN CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
  • ANTI-HUMAN ELT
  • ANTI-CFTR
  • ANTI-ABCC7
  • Anti-CFTR antibody produced in rabbit
  • ABCC7
  • cAMP- dependent chloride channel
  • Anti-ATP-binding cassette transporter sub-family C member 7
  • Anti-cAMP-dependent chloride channel
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