7218875

Connexin 43 Monoclonal Antibody (Connexin43 (1A)), eBioscience™, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer: Fischer Scientific

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Antigen

Connexin 43

Concentration

0.5 mg/mL

Classification

Monoclonal

Form

Liquid

Regulatory Status

RUO

Formulation

PBS with 0.09% sodium azide; pH 7.2

Gene Alias

alpha 1 connexin; AU042049; AVSD3; AW546267; CMDR; Cnx43; connexin 43; connexin43; connexin-43; cx43; Cx-43; cx43 protein; cx43a1; Cx43alpha1; CXA1; Cxn-43; DFNB38; EKVP; etID309742.9; gap junction 43 kDa heart protein; Gap junction alpha-1 protein; gap junction membrane channel protein; gap junction membrane channel protein alpha 1; gap junction protein; gap junction protein alpha 1; gap junction protein connexin 43; gap junction protein, alpha 1; gap junction protein, alpha 1, 43 kD (connexin 43); gap junction protein, alpha 1, 43kDa; gap junction protein, alpha 1, 43kDa (connexin 43); gja1; Gja-1; GJAL; HLHS1; HSS; Npm1; ODD; ODDD; ODOD; PPKCA; SDTY3; shf; Short fin protein; sof; stopsel; stp; Syndactyly type III; vascular smooth muscle connexin43; Vascular smooth muscle connexin-43; zfCx43.3

Gene Symbols

GJA1

Primary or Secondary

Primary

Content And Storage

4° C

Gene

GJA1

Clone

Connexin43 (1A)

Applications

Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Frozen), Immunohistochemistry (Paraffin), Western Blot

Conjugate

Unconjugated

Host Species

Mouse

Target Species

Human, Mouse, Rat

Gene Accession No.

P08050, P17302, P23242

Gene ID (Entrez)

14609, 24392, 2697

Isotype

IgG1 κ

Purification Method

Affinity chromatography

Product Type

Antibody

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Description

  • The Connexin43 MAb recognizes mouse Connexin 43
  • Connexins are a family of integral membrane proteins that form gap junction channels, which function to facilitate direct cell-cell communication
  • Gap junctions are comprised of two hemichannels, or connexons, which are made up of six connexin proteins
  • Over 20 connexin proteins have been identified and each combine to form either homomeric or heteromeric channels with different functional properties
  • Connexin 43 is expressed in many tissues, including the central nervous system, heart, and bone
  • Connexin 43 is the most abundant connexin found in the myocardium and is also the primary connexin expressed in astrocytes
  • Mutations in connexin 43 are associated with ocluodentodigital dysplasia, a rare developmental disorder characterized by craniofacial and limb abnormalities
  • Connexin 43 may also be a promising therapeutic target in the treatment of malignant melanomas and mammary gland tumors
  • The MAb Connexin43 also recognizes human and rat connexin 43
  • 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.