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Josephin-2 (L-12) 抗体: sc-109945

 |  データシート
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping within an internal region of Josephin-2 of human origin
  • recommended for detection of Josephin-2 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including bovine
  • blocking peptide, sc-109945 P
 
Additional Josephin 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 JOSD2 126119 19q13.33 Q8TAC2
n/a
マウス Josd2 66124 7 B4 Q9CR30
N/A
 
Set Currency

 注文情報
製品名カタログ #Unit価格数量追加Favorites
Josephin-2 (L-12) sc-109945 200 µg/ml $279
Josephin-2 (L-12) P sc-109945 P
(peptide)
100 µg/0.5 ml $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
Josephin-2 siRNA (h) sc-97479 10 µM $258
Josephin-2 siRNA (m) sc-146329 10 µM $258
Josephin-2 (h)-PR sc-97479-PR 10 µM $23
Josephin-2 (m)-PR sc-146329-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
Josephin-2 shRNA Plasmid (h) sc-97479-SH 20 µg $520
Josephin-2 shRNA Plasmid (m) sc-146329-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
Josephin-2 shRNA (h) Lentiviral Particles sc-97479-V 200 µl $625
Josephin-2 shRNA (m) Lentiviral Particles sc-146329-V 200 µl $625

Josephin-2 Background Information
Josephin-2, also known as JOSD2 (josephin domain containing 2), is a 188 amino acid protein that contains one josephin domain and is encoded by a gene that maps to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcå receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.