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Connexin 47 Polyclonal Antibody
商品货号: PLA015385
适 应 性: 人,大鼠,小鼠,
WB IF ELISA
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: GJC2
  • 蛋白名称: Gap junction gamma-2 protein
  • Human_gene_id: 57165
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57165
  • Human_swiss_prot_no: Q5T442
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q5T442/entry
  • Mouse_swiss_prot_no: Q8BQU6
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8BQU6
  • 特异性: Connexin 47 Polyclonal Antibody detects endogenous levels of Connexin 47 protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: GJC2; GJA12; Gap junction gamma-2 protein; Connexin-46.6; Cx46.6; Connexin-47; Cx47; Gap junction alpha-12 protein
  • 实测条带: 47kD
  • 功能: caution:It is uncertain whether Met-1 or Met-4 is the initiator.,disease:Defects in GJC2 are the cause of Leukodystrophy hypomyelinating type 2 (HLD2) [MIM:608804]; also known as Pelizaeus-Merzbacher-like disease autosomal recessive type 1. HLD2 is an autosomal recessive hypomyelinating leukodystrophy characterized by nystagmus, impaired motor development, ataxia, choreoathetotic movements, dysarthria and progressive spasticity.,function:One 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 role in myelination in central and peripheral nervous systems.,similarity:Belongs to the connexin family. Gamma-type subfamily.,subunit:A connexon is composed of a hexamer of connexins. Interacts with TJP1.,tissue specificity:Expressed in central nervous system, in sciatic nerve and sural nerve. Also detected in skeletal muscles.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
  • 组织表达: Expressed in central nervous system, in sciatic nerve and sural nerve. Also detected in skeletal muscles.
  • 科研货号: PLA015385
Connexin 47 Polyclonal Antibody
Catalog No PLA015385
Product information
  • 基因名称: GJC2
  • 蛋白名称: Gap junction gamma-2 protein
  • Human_gene_id: 57165
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57165
  • Human_swiss_prot_no: Q5T442
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q5T442/entry
  • Mouse_swiss_prot_no: Q8BQU6
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8BQU6
  • 特异性: Connexin 47 Polyclonal Antibody detects endogenous levels of Connexin 47 protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: GJC2; GJA12; Gap junction gamma-2 protein; Connexin-46.6; Cx46.6; Connexin-47; Cx47; Gap junction alpha-12 protein
  • 实测条带: 47kD
  • 功能: caution:It is uncertain whether Met-1 or Met-4 is the initiator.,disease:Defects in GJC2 are the cause of Leukodystrophy hypomyelinating type 2 (HLD2) [MIM:608804]; also known as Pelizaeus-Merzbacher-like disease autosomal recessive type 1. HLD2 is an autosomal recessive hypomyelinating leukodystrophy characterized by nystagmus, impaired motor development, ataxia, choreoathetotic movements, dysarthria and progressive spasticity.,function:One 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 role in myelination in central and peripheral nervous systems.,similarity:Belongs to the connexin family. Gamma-type subfamily.,subunit:A connexon is composed of a hexamer of connexins. Interacts with TJP1.,tissue specificity:Expressed in central nervous system, in sciatic nerve and sural nerve. Also detected in skeletal muscles.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
  • 组织表达: Expressed in central nervous system, in sciatic nerve and sural nerve. Also detected in skeletal muscles.
  • 科研货号: PLA015385
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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