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- rabbit polyclonal IgG, 100µg/ml
- recommended for detection of OASL of human origin by WB, IP, IF, IHC(P) and ELISA
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Ordering Information
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| Species |
Gene Name |
Gene ID |
Chromosome Location |
Isoform (mRNA) Accession # |
Protein Accession # |
OMIM™ Number |
| Human |
OASL |
8638 |
12q24.31 |
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Q15646
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603281 |
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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. |
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OASL (L-25)
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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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