ASXL1 antibody (AA 14-1541)

Catalog No. ABIN7870615

The Rabbit Polyclonal anti-ASXL1 antibody (ABIN7870615) specifically detects ASXL1 in WB, FACS and ELISA. The antibody is reactive with Human samples.

Quick Overview for ASXL1 antibody (AA 14-1541) (ABIN7870615)

Target: ASXL1 (Additional Sex Combs Like 1 (ASXL1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ASXL1 antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), ELISA

Product Details anti-ASXL1 Antibody

Binding Specificity: AA 14-1541

Purpose: ASXL1 Antibody

Purification: Affinity purified

Immunogen: Recombinant human protein (amino acids A14-R1541) was used as the immunogen for the ASXL1 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the ASXL1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the ASXL1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for ASXL1

Target: ASXL1 (Additional Sex Combs Like 1 (ASXL1))

Alternative Name: ASXL1

Background: Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene. This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants.

UniProt: Q8IXJ9

Pathways: Retinoic Acid Receptor Signaling Pathway