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磷酸化Connexin 43蛋白抗体

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产品名称: 磷酸化Connexin 43蛋白抗体
产品型号: Phospho-Connexin 43 (Ser368)
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

磷酸化Connexin 43蛋白抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。磷酸化Connexin 43蛋白抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


磷酸化Connexin 43蛋白抗体  的详细介绍

磷酸化Connexin 43蛋白抗体

规格:1mg/1ml

英文名: Phospho-Connexin 43 (Ser368)

别名: Connexin 43(phospho-Ser368); Connexin 43(phospho Ser368); Connexin 43(phospho S368); Connexin 43; Connexin43v Cx 43v CX43; DFNB38; Gap junction 43 kDa heart protein;Connexin-43; Gap junction alpha 1 p

分子量: 43kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated Synthesised phosphopeptide derived from human

交叉反应:Human, Mouse, Rat, Dog, Cow, Monkey,

细胞定位:细胞膜

磷酸化Connexin 43蛋白抗体产品介绍:background: 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 and heart malformations. [provided by RefSeq]. Function: Gap junction protein that acts as a regulator of bladder capacity. A gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. May play a critical role in the physiology of hearing by participating in磷酸化Connexin 43蛋白抗体 the recycling of potassium to the cochlear endolymph. Negative regulator of bladder functional capacity: acts by enhancing intercellular electrical and chemical transmission, thus sensitizing bladder muscles to cholinergic neural stimuli and causing them to contract. Subunit: A connexon is composed of a hexamer of connexins. Interacts (via C-terminus) with TJP1. Interacts (via C-terminus) with SRC (via SH3 domain). Interacts with UBQLN4. Interacts with SGSM3. Interacts with KIAA1432/CIP150. Interacts with CNST and CSNK1D. Subcellular Location: Cell membrane; Multi-pass membrane protein. Cell junction, gap junction. Tissue Specificity: Expressed in the heart and fetal cochlea. Post-translational modifications: Phosphorylated at Ser-368 by PRKCG; phosphorylation induces disassembly of gap junction plaques and inhibition of gap junction activity. Phosphorylation at Ser-325, Ser-328 and Ser-330 by CK1 modulates gap junction assembly. DISEASE: Defects in GJA1 are the cause of autosomal dominant oculodentodigital dysplasia (ODDD) [MIM:164200]; also known as oculodentoosseous dysplasia. ODDD is a highly penetrant syndrome presenting with craniofacial (ocular, nasal, dental) and limb dysmorphisms, spastic paraplegia, and neurodegeneration. Craniofacial anomalies tipically磷酸化Connexin 43蛋白抗体 include a thin nose with hypoplastic alae nasi, small anteverted nares, prominent columnella, and microcephaly. Brittle nails and hair abnormalities of hypotrichosis and slow growth are present. Ocular defects include microphthalmia, microcornea, cataracts, glaucoma, and optic atrophy. Syndactyly type 3 and conductive deafness can occur in some cases. Cardiac abnormalities are observed in rare instances. Similarity: Belongs to the connexin family. Alpha-type (group II) subfamily. Gene ID: 2697 Database links: Entrez Gene: 2697 Human Entrez Gene: 281193 Cow Entrez Gene: 403418 Dog Entrez Gene: 14609 Mouse Entrez Gene: 24392 Rat Omim: 121014 Human SwissProt: P18246 Cow SwissProt: Q6S9C0 Dog SwissProt: P17302 Human SwissProt: P23242 Mouse SwissProt: Q6TYA7 Rabbit SwissProt: P08050 Rat Unigene: 74471 Human Unigene: 378921 Mouse Unigene: 10346 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 间隙连接蛋白-43(Gap junction alpha-1 protein; GJA-1; (Vascular smooth muscle connexin-43))是构成细胞间的通道,小分子成份可以借此在细胞间扩散。Connexin-43也是心肌缝隙连接的主要蛋白之一。 此外,星形细胞、成纤维细胞、平滑肌和肾等组织也有表达Connexin 43.

磷酸化Connexin 43蛋白抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:心血管  细胞生物  神经生物学  信号转导  细胞粘附分子  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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