首页 > 抗体 > 一抗 > 其它 > GUC1A rabbit pAb
GUC1A rabbit pAb
商品货号: PLA009416
适 应 性: 人,小鼠
WB
¥600元
规格:
在线咨询
MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: GUCA1A C6orf131 GCAP GCAP1 GUCA1
  • 蛋白名称: GUC1A
  • Human_gene_id: 2978
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2978
  • Human_swiss_prot_no: P43080
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P43080/entry
  • Mouse_gene_id: 14913
  • Mouse_gene_link: https://www.uniprot.org/uniprot/14913
  • Mouse_swiss_prot_no: P43081
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P43081
  • 特异性: This antibody detects endogenous levels of GUC1A at Human/Mouse
  • 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: 22kD
  • 功能: disease:Defects in GUCA1A are the cause of cone dystrophy type 3 (COD3) [MIM:602093]. COD3 is an autosomal dominant cone dystrophy. Cone dystrophies are retinal dystrophies characterized by progressive degeneration of the cone photoreceptors with preservation of rod function, as indicated by electroretinogram. However, some rod involvement may be present in some cone dystrophies, particularly at late stage. Affected individuals suffer from photophobia, loss of visual acuity, color vision and central visual field. Another sign is the absence of macular lesions for many years. Cone dystrophies are distinguished from the cone-rod dystrophies, in which some loss of peripheral vision also occurs.,function:Stimulates guanylyl cyclase 1 (GC1) when free calcium ions concentration is low and inhibits GC1 when free calcium ions concentration is elevated. This Ca(2+)-sensitive regulation of GC is a key event in recovery of the dark state of rod photoreceptors following light exposure.,miscellaneous:Binds three calcium ions.,online information:Retina International's Scientific Newsletter,similarity:Contains 4 EF-hand domains.,tissue specificity:Retina; cone outer and inner segments, in particular, in disk membrane regions, and to a lesser extent rod inner and outer segments.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Membrane; Lipid-anchor . Photoreceptor inner segment . Cell projection, cilium, photoreceptor outer segment . Present at higher levels in cone than in rod outer segments (PubMed:9620085). Subcellular location is not affected by light or dark conditions. .
  • 组织表达: In the retina, it is expressed in rod and cone photoreceptors.
  • 科研货号: PLA009416
GUC1A rabbit pAb
Catalog No PLA009416
Product information
  • 发货日期: 7
  • 基因名称: GUCA1A C6orf131 GCAP GCAP1 GUCA1
  • 蛋白名称: GUC1A
  • Human_gene_id: 2978
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2978
  • Human_swiss_prot_no: P43080
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P43080/entry
  • Mouse_gene_id: 14913
  • Mouse_gene_link: https://www.uniprot.org/uniprot/14913
  • Mouse_swiss_prot_no: P43081
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P43081
  • 特异性: This antibody detects endogenous levels of GUC1A at Human/Mouse
  • 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: 22kD
  • 功能: disease:Defects in GUCA1A are the cause of cone dystrophy type 3 (COD3) [MIM:602093]. COD3 is an autosomal dominant cone dystrophy. Cone dystrophies are retinal dystrophies characterized by progressive degeneration of the cone photoreceptors with preservation of rod function, as indicated by electroretinogram. However, some rod involvement may be present in some cone dystrophies, particularly at late stage. Affected individuals suffer from photophobia, loss of visual acuity, color vision and central visual field. Another sign is the absence of macular lesions for many years. Cone dystrophies are distinguished from the cone-rod dystrophies, in which some loss of peripheral vision also occurs.,function:Stimulates guanylyl cyclase 1 (GC1) when free calcium ions concentration is low and inhibits GC1 when free calcium ions concentration is elevated. This Ca(2+)-sensitive regulation of GC is a key event in recovery of the dark state of rod photoreceptors following light exposure.,miscellaneous:Binds three calcium ions.,online information:Retina International's Scientific Newsletter,similarity:Contains 4 EF-hand domains.,tissue specificity:Retina; cone outer and inner segments, in particular, in disk membrane regions, and to a lesser extent rod inner and outer segments.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Membrane; Lipid-anchor . Photoreceptor inner segment . Cell projection, cilium, photoreceptor outer segment . Present at higher levels in cone than in rod outer segments (PubMed:9620085). Subcellular location is not affected by light or dark conditions. .
  • 组织表达: In the retina, it is expressed in rod and cone photoreceptors.
  • 科研货号: PLA009416
  • 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.
普拉特泽实验室电话助手

4006916686

扫码咨询