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CRGC rabbit pAb
商品货号: PLA009780
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: CRYGC CRYG3
  • 蛋白名称: CRGC
  • Human_gene_id: 1420
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1420
  • Human_swiss_prot_no: P07315
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P07315/entry
  • Mouse_gene_id: 12966
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12966
  • Mouse_swiss_prot_no: Q61597
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q61597
  • Rat_gene_id: 24277
  • Rat_gene_link: https://www.uniprot.org/uniprot/24277
  • Rat_swiss_prot_no: P02529
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P02529
  • 特异性: This antibody detects endogenous levels of CRGC at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 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
  • 分子量: 19kD
  • 功能: disease:Crystallins do not turn over as the lens ages, providing ample opportunity for post-translational modifications or oxidations. These modifications may change crystallin solubility properties and favor senile cataract.,disease:Defects in CRYGC are a cause of autosomal dominant cataract [MIM:604219]. Cataract is an opacification of the eye lens that frequently results in visual impairment or blindness during infancy and early childhood.,disease:Defects in CRYGC are a cause of Coppock-like cataract (CCL) [MIM:604307]. The Coppock cataract refers to a congenital pulverulent disk-like opacity involving the embryonal and fetal nucleus with many tiny white dots in the lamellar portion of the lens. It is usually bilateral and dominantly inherited.,disease:Defects in CRYGC are the cause of variable zonular pulverulent cataract [MIM:123680].,domain:Has a two-domain beta-structure, folded into four very similar Greek key motifs.,function:Crystallins are the dominant structural components of the vertebrate eye lens.,mass spectrometry: PubMed:12876325,similarity:Belongs to the beta/gamma-crystallin family.,similarity:Contains 4 beta/gamma crystallin 'Greek key' domains.,subunit:Monomer.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: nucleus,cytoplasm,
  • 科研货号: PLA009780
CRGC rabbit pAb
Catalog No PLA009780
Product information
  • 发货日期: 7
  • 基因名称: CRYGC CRYG3
  • 蛋白名称: CRGC
  • Human_gene_id: 1420
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1420
  • Human_swiss_prot_no: P07315
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P07315/entry
  • Mouse_gene_id: 12966
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12966
  • Mouse_swiss_prot_no: Q61597
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q61597
  • Rat_gene_id: 24277
  • Rat_gene_link: https://www.uniprot.org/uniprot/24277
  • Rat_swiss_prot_no: P02529
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P02529
  • 特异性: This antibody detects endogenous levels of CRGC at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 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
  • 分子量: 19kD
  • 功能: disease:Crystallins do not turn over as the lens ages, providing ample opportunity for post-translational modifications or oxidations. These modifications may change crystallin solubility properties and favor senile cataract.,disease:Defects in CRYGC are a cause of autosomal dominant cataract [MIM:604219]. Cataract is an opacification of the eye lens that frequently results in visual impairment or blindness during infancy and early childhood.,disease:Defects in CRYGC are a cause of Coppock-like cataract (CCL) [MIM:604307]. The Coppock cataract refers to a congenital pulverulent disk-like opacity involving the embryonal and fetal nucleus with many tiny white dots in the lamellar portion of the lens. It is usually bilateral and dominantly inherited.,disease:Defects in CRYGC are the cause of variable zonular pulverulent cataract [MIM:123680].,domain:Has a two-domain beta-structure, folded into four very similar Greek key motifs.,function:Crystallins are the dominant structural components of the vertebrate eye lens.,mass spectrometry: PubMed:12876325,similarity:Belongs to the beta/gamma-crystallin family.,similarity:Contains 4 beta/gamma crystallin 'Greek key' domains.,subunit:Monomer.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: nucleus,cytoplasm,
  • 科研货号: PLA009780
  • 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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