PROSER2 antibody (PE-Cy7)

Catalog No. ABIN1437541

This Rabbit Polyclonal antibody specifically detects PROSER2 in WB. It exhibits reactivity toward Human, Mouse, Rat and Pig.

Quick Overview for PROSER2 antibody (PE-Cy7) (ABIN1437541)

Target: PROSER2 (Proline and Serine-Rich Protein 2 (PROSER2))

Reactivity: Human, Mouse, Rat, Pig

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PROSER2 antibody is conjugated to PE-Cy7

Application: Western Blotting (WB)

Product Details anti-PROSER2 Antibody (PE-Cy7)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C10orf47

Isotype: IgG

Application Details

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for PROSER2

Target: PROSER2 (Proline and Serine-Rich Protein 2 (PROSER2))

Alternative Name: C10orf47

Background:

Synonyms: C10orf47, Chromosome 10 open reading frame 47, CJ047_HUMAN, Hypothetical protein LOC254427, MGC35403, Uncharacterized protein C10orf47.

Background: C10orf47 is a 435 amino acid protein that exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 10. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Molecular Weight: 46kDa

Gene ID: 254427