儲(chǔ)存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆號(hào): PT0467R
特異性: Endogenous
基因名稱: GJA1
蛋白名稱: Gap junction alpha-1 protein
別名: GJA1;GJAL;Gap junction alpha-1 protein;Connexin-43;Cx43;Gap junction 43 kDa heart protein
Organism-1: Human
基因ID-1: 2697
SwissProt-1: P17302
Organism-2: Mouse
基因ID-2: 14609
SwissProt-2: P23242
Organism-3: Rat
基因ID-3: 24392
SwissProt-3: P08050
背景: This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014],
儲(chǔ)存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆號(hào): PT0467R
特異性: Endogenous
基因名稱: GJA1
蛋白名稱: Gap junction alpha-1 protein
別名: GJA1;GJAL;Gap junction alpha-1 protein;Connexin-43;Cx43;Gap junction 43 kDa heart protein
Organism-1: Human
基因ID-1: 2697
SwissProt-1: P17302
Organism-2: Mouse
基因ID-2: 14609
SwissProt-2: P23242
Organism-3: Rat
基因ID-3: 24392
SwissProt-3: P08050
背景: This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014],
細(xì)胞定位: Membrane
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