DDX39B antibody

Catalog No. ABIN7266696

Product Details anti-DDX39B Antibody

Target: DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This DDX39B antibody is un-conjugated

Application: Immunohistochemistry (IHC), Western Blotting (WB)

Purpose: UAP56/DDX39B Rabbit mAb

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Monoclonal Antibodies

Purification: Affinity purification

Immunogen: A synthesized peptide derived from human UAP56/DDX39B

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for DDX39B

Target: DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

Alternative Name: DDX39B (DDX39B Products)

Synonyms: BAT1 antibody, D6S81E antibody, UAP56 antibody, Bat1 antibody, Bat1a antibody, p47 antibody, 0610030D10Rik antibody, AI428441 antibody, Bat-1 antibody, D17H6S81E antibody, D17H6S81E-1 antibody, D6S81Eh antibody, bat1 antibody, zgc:63773 antibody, DExD-box helicase 39B antibody, DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B antibody, DDX39B antibody, Ddx39b antibody, ddx39b antibody

Background: This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13 kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011],BAT1, D6S81E, UAP56,Epigenetics & Nuclear Signaling,DDX39B

Molecular Weight: 45kDa

Gene ID: 7919

UniProt: Q13838

Pathways: Ribonucleoprotein Complex Subunit Organization