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Zwilch (NB-C38) 抗体: sc-135615

 |  データシート
  • mouse monoclonal IgG1, 100µg/ml
  • recommended for detection of Zwilch of human origin by WB, IP and ELISA
 
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WB   IP   siRNA  
 
Species 遺伝子名 Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
ヒト ZWILCH 55055 15q22.31 Q9H900
609984
 
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 注文情報
製品名カタログ #Unit価格数量追加Favorites
Zwilch (NB-C38) sc-135615 100 µg/ml $279
 siRNA遺伝子サイレンサー (click product name for more information)
製品名カタログ #Unit価格数量追加Favorites
Zwilch siRNA (h) sc-63261 10 µM $258
Zwilch (h)-PR sc-63261-PR 10 µM $23
 shRNAプラスミド (click product name for more information)
製品名カタログ #Unit価格数量追加Favorites
Zwilch shRNA Plasmid (h) sc-63261-SH 20 µg $520
 shRNA レンチウイルス粒子 (click product name for more information)
製品名カタログ #Unit価格数量追加Favorites
Zwilch shRNA (h) Lentiviral Particles sc-63261-V 200 µl $625

Zwilch Background Information
Zwilch is the human homolog of the Drosophila Zwilch protein. The Drosophila Zwilch forms a complex with both ROD Rough Deal) and ZWINT (Zeste-White 10, also designated ZW10) proteins. This complex is important for chromosome segregation because it recruits cytoplasmic Dynein to the kinetochore and plays a crucial role in the spindle checkpoint. The role of Zwilch in complex is thought to be evolutionarily conserved because the human homologs of Zwilch, ZWINT and ROD coimmunoprecipitate in a human cell line called HeLa. The human Zwilch, ZWINT and ROD complex localizes to the kinetochores at prometaphase. Mutations were discovered in Zwilch, ZWINT and ROD during a screen for mutations in alleles encoding putative chromosome instability genes in cases of human colorectal cancer. These mutations may contribute in part to the chromosomal instability phenotype of colorectal tumor cells.

Zwilch (NB-C38)
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Zwilch (NB-C38): sc-135615. Western blot analysis of Zwilch expression in human Zwilch transfected (A) and non-transfected (B) 293T whole cell lysates.
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