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OASL (L-25) Antibody: sc-130832

 |  Datasheet
  • rabbit polyclonal IgG, 100µg/ml
  • recommended for detection of OASL of human origin by WB, IP, IF, IHC(P) and ELISA
 
Additional OASL Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   IF   IHC(P)   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human OASL 8638 12q24.31 Q15646
603281
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
OASL (L-25) sc-130832 100 µg/ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
OASL siRNA (h) sc-95857 10 µM $258
OASL (h)-PR sc-95857-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
OASL shRNA Plasmid (h) sc-95857-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
OASL shRNA (h) Lentiviral Particles sc-95857-V 200 µl $625
 WB Positive Control Cell Lysate (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
HL-60 Whole Cell Lysate sc-2209 500 µg/200 µl $104

OASL Background Information
OASL (2'-5'-oligoadenylate synthetase-like), also known as p59OASL or TRIP14 (thyroid receptor-interacting protein 14), is a 514 amino acid protein that exists as two alternatively spliced isoforms, designated p56 and p30, and contains two ubiquitin-like domains. Expressed in a variety of tissues with highest levels present in colon, stomach and testis, OASL interacts with the ligand binding domain of the thyroid receptor (TR) and is able to bind double-stranded RNA and DNA, possibly playing a role in RNA degradation and the overall inhibition of protein synthesis. The gene encoding OASL maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

OASL (L-25)
Click on image to enlarge
OASL (L-25): sc-130832. Immunoperoxidase staining of formalin-fixed, paraffin-embedded human breast carcinoma tissue showing cytoplasmic localization.
OASL (L-25): sc-130832. Western blot analysis of OASL expression in HL-60 whole cell lysate.
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