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WFDC1 (W-15) 抗体: sc-109157

 |  データシート
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping within an internal region of WFDC1 of human origin
  • recommended for detection of WFDC1 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, bovine, porcine and avian
  • blocking peptide, sc-109157 P
 
Additional WFDC 抗体 ...
 
注文情報
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WB   IF   siRNA  
 
Species 遺伝子名 Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
ヒト WFDC1 58189 16q24.1 Q9HC57
605322
マウス Wfdc1 67866 8 E1 Q9ESH5
N/A
 
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 注文情報
製品名カタログ #Unit価格数量追加Favorites
WFDC1 (W-15) sc-109157 200 µg/ml $279
WFDC1 (W-15) P sc-109157 P
(peptide)
100 µg/0.5ml $61
 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
WFDC1 siRNA (h) sc-93280 10 µM $258
WFDC1 siRNA (m) sc-155334 10 µM $258
WFDC1 (h)-PR sc-93280-PR 10 µM $23
WFDC1 (m)-PR sc-155334-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
WFDC1 shRNA Plasmid (h) sc-93280-SH 20 µg $520
WFDC1 shRNA Plasmid (m) sc-155334-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
WFDC1 shRNA (h) Lentiviral Particles sc-93280-V 200 µl $625
WFDC1 shRNA (m) Lentiviral Particles sc-155334-V 200 µl $625

WFDC1 Background Information
The WAP domain (also referred to as the WAP-type four-disulfide core domain), is a signature protein motif that contains eight cysteine residues which form disulfide bonds and may exhibit protease inhibitor activity. WFDC1 (WAP four-disulfide core domain 1), also known as PS20, is a 220 amino acid secreted protein that contains one WAP domain and is thought to possess growth inhibitory activity. The gene encoding WFDC1 maps to a region on human chromosome 16 that is often lost or mutated in several cancers, including breast, prostate and hepatocellular carcinomas, suggesting a role for native WFDC1 in tumor suppression. Human chromosome 16, on which the WFDC1 gene is located, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.