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XYLB (A-19) Antibody: sc-99722

 |  Datasheet
  • rabbit polyclonal IgG, 100µg/ml
  • epitope mapping near the C-terminus of XYLB of human origin
  • recommended for detection of XYLB of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine and canine
  • blocking peptide, sc-99722 P
 
Additional XYLB Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   IF   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human XYLB 9942 3p22.2 O75191
604049
 
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 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
XYLB (A-19) sc-99722 100 µg/ml $279
XYLB (A-19) P sc-99722 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
XYLB siRNA (h) sc-78008 10 µM $258
XYLB siRNA (m) sc-155398 10 µM $258
XYLB (h)-PR sc-78008-PR 10 µM $23
XYLB (m)-PR sc-155398-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
XYLB shRNA Plasmid (h) sc-78008-SH 20 µg $520
XYLB shRNA Plasmid (m) sc-155398-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
XYLB shRNA (h) Lentiviral Particles sc-78008-V 200 µl $625
XYLB shRNA (m) Lentiviral Particles sc-155398-V 200 µl $625

XYLB Background Information
XYLB (Xylulose kinase or Xylulokinase) is a 536 amino acid protein that utlilizes ATP to phosphorylate D-xylulose and may play a role in energy metabolism. The XYLB gene resides on chromosome 3, which contains about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

XYLB (A-19)
Click on image to enlarge
XYLB (A-19): sc-99722. Western blot analysis of XYLB expression in HeLa whole cell lysate.
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