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RD3 rabbit pAb
商品貨號: PLA021161
適 應 性: 人,小鼠
WB IHC ELISA
¥600元
規格:
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MSDS
說明書
商品描述
  • 基因名稱: RD3 C1orf36
  • 蛋白名稱: RD3
  • Human_gene_id: 343035
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=343035
  • Human_swiss_prot_no: Q7Z3Z2
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q7Z3Z2/entry
  • Mouse_gene_id: 74023
  • Mouse_gene_link: https://www.uniprot.org/uniprot/74023
  • Mouse_swiss_prot_no: Q8BRE0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8BRE0
  • 特異性: This antibody detects endogenous levels of RD3 at Human/Mouse
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 21kD
  • 功能: disease:Defects in RD3 are the cause of Leber congenital amaurosis type 12 (LCA12) [MIM:610612]. LCA designates a clinically and genetically heterogeneous group of childhood retinal degenerations, generally inherited in an autosomal recessive manner. Affected infants have little or no retinal photoreceptor function as tested by electroretinography. LCA represents the most common genetic cause of congenital visual impairment in infants and children.,tissue specificity:Preferentially expressed in retina.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Cell projection, cilium, photoreceptor outer segment . Photoreceptor inner segment . Endosome . Nucleus . Cytoplasm . Cytoplasm, perinuclear region . Colocalizes with GUCY2E and GUCY2F in rods and cones photoreceptors. Colocalizes with GUK1 in photoreceptor inner segments and to a lesser extent in the outer plexiform layer (By similarity). Strong dot-like perinuclear staining in the epithelial cells (PubMed:29030614). .
  • 組織表達: Expressed in retina (PubMed:12914764). Widely expressed (at protein level) (PubMed:29030614). In the retina the strongest immunoreactivity is detected in the inner half of the cytoplasmic portion of the photoreceptor layer, where rods and cones are found, and the external half of the outer plexiform layer (at protein level) (PubMed:29030614).
  • 科研貨號: PLA021161
RD3 rabbit pAb
Catalog No PLA021161
Product information
  • 基因名稱: RD3 C1orf36
  • 蛋白名稱: RD3
  • Human_gene_id: 343035
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=343035
  • Human_swiss_prot_no: Q7Z3Z2
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q7Z3Z2/entry
  • Mouse_gene_id: 74023
  • Mouse_gene_link: https://www.uniprot.org/uniprot/74023
  • Mouse_swiss_prot_no: Q8BRE0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8BRE0
  • 特異性: This antibody detects endogenous levels of RD3 at Human/Mouse
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 21kD
  • 功能: disease:Defects in RD3 are the cause of Leber congenital amaurosis type 12 (LCA12) [MIM:610612]. LCA designates a clinically and genetically heterogeneous group of childhood retinal degenerations, generally inherited in an autosomal recessive manner. Affected infants have little or no retinal photoreceptor function as tested by electroretinography. LCA represents the most common genetic cause of congenital visual impairment in infants and children.,tissue specificity:Preferentially expressed in retina.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Cell projection, cilium, photoreceptor outer segment . Photoreceptor inner segment . Endosome . Nucleus . Cytoplasm . Cytoplasm, perinuclear region . Colocalizes with GUCY2E and GUCY2F in rods and cones photoreceptors. Colocalizes with GUK1 in photoreceptor inner segments and to a lesser extent in the outer plexiform layer (By similarity). Strong dot-like perinuclear staining in the epithelial cells (PubMed:29030614). .
  • 組織表達: Expressed in retina (PubMed:12914764). Widely expressed (at protein level) (PubMed:29030614). In the retina the strongest immunoreactivity is detected in the inner half of the cytoplasmic portion of the photoreceptor layer, where rods and cones are found, and the external half of the outer plexiform layer (at protein level) (PubMed:29030614).
  • 科研貨號: PLA021161
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