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OLIG2 antibody (AA 152-180)
This Rabbit Polyclonal antibody specifically detects OLIG2 in WB and ELISA. It exhibits reactivity toward Mouse.
Quick Overview for OLIG2 antibody (AA 152-180) (ABIN3032092)
Target
See all OLIG2 Antibodies
OLIG2
(Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
Reactivity
All reactivities for OLIG2 antibodies
Mouse
Host
All hosts for OLIG2 antibodies
Rabbit
Clonality
All clonalities for OLIG2 antibodies
Polyclonal
Conjugate
All conjugates for OLIG2 antibodies
This OLIG2 antibody is un-conjugated
Application
All applications for OLIG2 antibodies
Western Blotting (WB), ELISA
Product Details anti-OLIG2 Antibody
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Binding Specificity
All epitopes for OLIG2 antibodies
AA 152-180
Cross-Reactivity (Details)
Expected species reactivity: Chicken
Purification
Antigen affinity purified
Immunogen
A portion of amino acids 152-180 from the human protein was used as the immunogen for this Olig2 antibody.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
Titration of the Olig2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
In 1X PBS pH 7.4 with 0.09 % sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Aliquot the Olig2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
Target Details for OLIG2
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Target
OLIG2
(Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
Alternative Name
Olig2
Background
This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14,21)(q11.2,q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq].
UniProt
Q13516
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