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Anti-Rat Connexin 37 (Cx37) IgG #2 | Gentaur

€340.00
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SKU:
15-CX37B12-A-GEN
Availability:
IN STOCK
Size:
100 µg
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Product Description

Anti-Rat Connexin 37 (Cx37) IgG #2

Species Reactivity Mouse, Rat

Published species Human, Mouse, Rat

Host/Isotype Mouse / IgG1

Class Monoclonal

Type Antibody

Clone 3D8A5

Immunogen Synthetic peptide derived from rat Connexin 43.

Conjugate Unconjugated

Form Liquid

Concentration 0.5 mg/mL

Purification Protein

A Storage buffer PBS, pH 7.4

Contains 0.1% sodium azide

Storage conditions -20°C

RRID AB_2533207

Target Information

Connexin 43 (Cx43) is a member of the gap junction protein family. Connexins assemble as a hexamer and are transported to the plasma membrane to create a hemichannel that can associate with hemichannels on nearby cells to create cell-to-cell channels. Clusters of these channels assemble to make gap junctions. Gap junction communication is important in development and regulation of cell growth.

Phosphorylation of Cx43 is important in regulating assembly and function of gap junctions. Ser368 of Cx43 is phosphorylated by protein kinase C (PKC) after activation by phorbol esters, which decreases cell-to-cell communication. Src can interact with and phosphorylate Cx43 to alter gap junction communication. GFAP are membrane-spanning proteins that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta.

Connexin 43 is the major protein of gap junctions in the heart, and gap junctions are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. Connexin 43 is also targeted by several protein kinases that regulate myocardial cell-cell coupling.

A related intron-less connexin 43 pseudogene, GJA1P, has been mapped to chromosome 5. Mutations in the GFAP gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy, oculodentodigital dysplasia and heart malformations. Alternatively spliced transcript variants of GFAP have been found.

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