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Goat polyclonal to OAS2
HumanPredicted to work with:
Synthetic peptide corresponding to Human OAS2 aa 357-371 (internal sequence). (NP_058197.2).
Database link: P29728
- Human breast tissue; Daudi, K562 and Jurkat cell lysates.
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Preservative: 0.02% Sodium azide
Constituents: 99% Tris buffered saline, 0.5% BSA
Concentration information loading...
Immunogen affinity purified
Our Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
||Use a concentration of 5 µg/ml.
||Use a concentration of 0.3 - 1 µg/ml. Detects a band of approximately 70 kDa (predicted molecular weight: 82, 79 kDa).
May play a role in mediating resistance to virus infection, control of cell growth, differentiation, and apoptosis.
Belongs to the 2-5A synthase family.
Mitochondrion. Nucleus. Microsome. Endoplasmic reticulum. Associated with different subcellular fractions such as mitochondrial, nuclear, and rough/smooth microsomal fractions.
Information by UniProt
- (2-5'')oligo(A) synthase 2 antibody
- (2-5')oligo(A) synthetase 2 antibody
- 2''-5''-oligoadenylate synthase 2 antibody
Western blot - Anti-OAS2 antibody (ab195968)
All lanes :
Anti-OAS2 antibody (ab195968) at 0.3 µg/mlLane 1 :
Daudi cell lysate (in RIPA buffer)Lane 2 :
Jurkat cell lysate (in RIPA buffer)Lane 3 :
K562 cell lysate (in RIPA buffer)
Lysates/proteins at 35 µg per lane.
Developed using the ECL techniquePredicted band size :
82, 79 kDaObserved band size :
70 kDa (why is the actual band size different from the predicted?
Primary incubation was 1 hour.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OAS2 antibody (ab195968)
Immunohistochemical analysis of formalin-fixed, paraffin-embedded Human breast tissue labeling OAS2 with ab195968 at 5 µg/ml.
has not yet been referenced specifically in any publications.
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