PABPC5 antibody

Catalog No. ABIN7467563

This anti-PABPC5 antibody is a Rabbit Polyclonal antibody detecting PABPC5 in WB and IHC (p). Suitable for Human.

Quick Overview for PABPC5 antibody (ABIN7467563)

Target: PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PABPC5 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-PABPC5 Antibody

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human PABPC5. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: U87-MG , A431 , HeLa , HepG2 , mouse brain , rat brain

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for PABPC5

Target: PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))

Alternative Name: poly(A) binding protein cytoplasmic 5

Background: Poly(A) binding protein cytoplasmic 5 , PABP5,This gene encodes a protein that binds to the polyA tail found at the 3' end of most eukaryotic mRNAs. It is thought to play a role in the regulation of mRNA metabolic processes in the cytoplasm. This gene is located in a gene-poor region within the X-specific 13d-sY43 subinterval of the chromosome Xq21.3/Yp11.2 homology block. It is located close to translocation breakpoints associated with premature ovarian failure, and is therefore a potential candidate gene for this disorder. [provided by RefSeq]

Molecular Weight: 43 kDa

Gene ID: 140886

UniProt: Q96DU9