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首頁 > 抗體 > 一抗 > 其它 > Collagen XVIII α1 (Cleaved-His1572) rabbit pAb
Collagen XVIII α1 (Cleaved-His1572) rabbit pAb
商品貨號: PLA004415
適 應(yīng) 性: 人,小鼠
WB ELISA
¥600元
規(guī)格:
在線咨詢
MSDS
說明書
商品描述
  • 基因名稱: COL18A1
  • 蛋白名稱: Collagen XVIII α1 (Cleaved-His1572)
  • Human_gene_id: 80781
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=80781
  • Human_swiss_prot_no: P39060
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P39060/entry
  • Mouse_gene_id: 12822
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12822
  • Mouse_swiss_prot_no: P39061
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P39061
  • 特異性: This antibody detects endogenous levels of Human,Mouse Collagen XVIII α1 (Cleaved-His1572, protein was cleaved amino acid sequence between 1571-1572 )
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:1000-2000 ELISA 1:5000-20000
  • 純化工藝: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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
  • 其他名稱: Collagen alpha-1(XVIII) chain [Cleaved into: Endostatin]
  • 實測條帶: 20 200kD
  • 功能: disease:Defects in COL18A1 are a cause of Knobloch syndrome (KNO) [MIM:267750]. KNO is an autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele.,function:COLA18A probably plays a major role in determining the retinal structure as well as in the closure of the neural tube.,function:Endostatin potently inhibits endothelial cell proliferation and angiogenesis. May inhibit angiogenesis by binding to the heparan sulfate proteoglycans involved in growth factor signaling.,polymorphism:There is an association between a polymorphism in position 1675 and prostate cancer. Heterozygous Asn-1675 individuals have a 2.5 times increased chance of developing prostate cancer as compared with homozygous Asp-1675 individuals.,PTM:Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.,similarity:Belongs to the multiplexin collagen family.,similarity:Contains 1 FZ (frizzled) domain.,similarity:Contains 1 TSP N-terminal (TSPN) domain.,tissue specificity:Present in multiple organs with highest levels in liver, lung and kidney.,
  • 相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3062
  • 細(xì)胞定位: Secreted, extracellular space, extracellular matrix . Secreted, extracellular space, extracellular matrix, basement membrane .; [Non-collagenous domain 1]: Secreted, extracellular space, extracellular matrix, basement membrane . Secreted .; [Endostatin]: Secreted . Secreted, extracellular space, extracellular matrix, basement membrane .
  • 組織表達(dá): Present in multiple organs with highest levels in liver, lung and kidney.
  • 科研貨號: PLA004415
Collagen XVIII α1 (Cleaved-His1572) rabbit pAb
Catalog No PLA004415
Product information
  • 基因名稱: COL18A1
  • 蛋白名稱: Collagen XVIII α1 (Cleaved-His1572)
  • Human_gene_id: 80781
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=80781
  • Human_swiss_prot_no: P39060
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P39060/entry
  • Mouse_gene_id: 12822
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12822
  • Mouse_swiss_prot_no: P39061
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P39061
  • 特異性: This antibody detects endogenous levels of Human,Mouse Collagen XVIII α1 (Cleaved-His1572, protein was cleaved amino acid sequence between 1571-1572 )
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:1000-2000 ELISA 1:5000-20000
  • 純化工藝: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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
  • 其他名稱: Collagen alpha-1(XVIII) chain [Cleaved into: Endostatin]
  • 實測條帶: 20 200kD
  • 功能: disease:Defects in COL18A1 are a cause of Knobloch syndrome (KNO) [MIM:267750]. KNO is an autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele.,function:COLA18A probably plays a major role in determining the retinal structure as well as in the closure of the neural tube.,function:Endostatin potently inhibits endothelial cell proliferation and angiogenesis. May inhibit angiogenesis by binding to the heparan sulfate proteoglycans involved in growth factor signaling.,polymorphism:There is an association between a polymorphism in position 1675 and prostate cancer. Heterozygous Asn-1675 individuals have a 2.5 times increased chance of developing prostate cancer as compared with homozygous Asp-1675 individuals.,PTM:Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.,similarity:Belongs to the multiplexin collagen family.,similarity:Contains 1 FZ (frizzled) domain.,similarity:Contains 1 TSP N-terminal (TSPN) domain.,tissue specificity:Present in multiple organs with highest levels in liver, lung and kidney.,
  • 相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3062
  • 細(xì)胞定位: Secreted, extracellular space, extracellular matrix . Secreted, extracellular space, extracellular matrix, basement membrane .; [Non-collagenous domain 1]: Secreted, extracellular space, extracellular matrix, basement membrane . Secreted .; [Endostatin]: Secreted . Secreted, extracellular space, extracellular matrix, basement membrane .
  • 組織表達(dá): Present in multiple organs with highest levels in liver, lung and kidney.
  • 科研貨號: PLA004415
  • Hunan UPT Biotechnology Co.,Ltd
    Website:m.hyjdss.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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