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PCD19 rabbit pAb
商品貨號: PLA020921
適 應 性: 人,小鼠
WB IHC
¥600元
規格:
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MSDS
說明書
商品描述
  • 基因名稱: PCDH19 KIAA1313
  • 蛋白名稱: PCD19
  • Human_gene_id: 57526
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57526
  • Human_swiss_prot_no: Q8TAB3
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q8TAB3/entry
  • Mouse_gene_id: 279653
  • Mouse_gene_link: https://www.uniprot.org/uniprot/279653
  • Mouse_swiss_prot_no: Q80TF3
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q80TF3
  • 特異性: This antibody detects endogenous levels of PCD19 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
  • 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: 126kD
  • 功能: developmental stage:Expressed in developing cortical plate, amygdala and subcortical regions and in the ganglionic eminence.,disease:Defects in PCDH19 are the cause of epilepsy, female-restricted, with mental retardation (EFMR) [MIM:300088]; also known as convulsive disorder and mental retardation. EFMR is a condition characterized by seizure onset in infancy or early childhood and cognitive impairment. The disorder is sex-limited, with the phenotype being restricted to females. Males are apparently spared.,function:Potential calcium-dependent cell-adhesion protein.,similarity:Contains 6 cadherin domains.,tissue specificity:Moderately expressed in all regions of the brain examined, with lowest levels found in the cerebellum. Moderate expression is also found in ovary, and low expression in all other tissues tested. Also detected in primary skin fibroblast.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Cell membrane ; Single-pass type I membrane protein .
  • 組織表達: Moderately expressed in all regions of the brain examined, with lowest levels found in the cerebellum. Moderate expression is also found in ovary, and low expression in all other tissues tested. Also detected in primary skin fibroblast.
  • 科研貨號: PLA020921
PCD19 rabbit pAb
Catalog No PLA020921
Product information
  • 基因名稱: PCDH19 KIAA1313
  • 蛋白名稱: PCD19
  • Human_gene_id: 57526
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57526
  • Human_swiss_prot_no: Q8TAB3
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q8TAB3/entry
  • Mouse_gene_id: 279653
  • Mouse_gene_link: https://www.uniprot.org/uniprot/279653
  • Mouse_swiss_prot_no: Q80TF3
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q80TF3
  • 特異性: This antibody detects endogenous levels of PCD19 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
  • 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: 126kD
  • 功能: developmental stage:Expressed in developing cortical plate, amygdala and subcortical regions and in the ganglionic eminence.,disease:Defects in PCDH19 are the cause of epilepsy, female-restricted, with mental retardation (EFMR) [MIM:300088]; also known as convulsive disorder and mental retardation. EFMR is a condition characterized by seizure onset in infancy or early childhood and cognitive impairment. The disorder is sex-limited, with the phenotype being restricted to females. Males are apparently spared.,function:Potential calcium-dependent cell-adhesion protein.,similarity:Contains 6 cadherin domains.,tissue specificity:Moderately expressed in all regions of the brain examined, with lowest levels found in the cerebellum. Moderate expression is also found in ovary, and low expression in all other tissues tested. Also detected in primary skin fibroblast.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Cell membrane ; Single-pass type I membrane protein .
  • 組織表達: Moderately expressed in all regions of the brain examined, with lowest levels found in the cerebellum. Moderate expression is also found in ovary, and low expression in all other tissues tested. Also detected in primary skin fibroblast.
  • 科研貨號: PLA020921
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.zjgzfxx.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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