C10orf88 antibody (FITC)

Catalog No. ABIN1404572

The Rabbit Polyclonal anti-C10orf88 antibody has been validated for WB and IF (p). It is suitable to detect C10orf88 in samples from Human, Mouse and Rat.

Quick Overview for C10orf88 antibody (FITC) (ABIN1404572)

Target: C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C10orf88 antibody is conjugated to FITC

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C10orf88 Antibody (FITC)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C10orf88

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

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: ProClin

Precaution of Use: This product contains ProClin: 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 C10orf88

Target: C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))

Alternative Name: C10orf88

Background:

Synonyms: Chromosome 10 open reading frame 88, CJ088_HUMAN, Em:AC073585.5, FLJ13490, Hypothetical protein LOC80007, Uncharacterized protein C10orf88.

Background: C10orf88 is a 445 amino acid protein encoded by a gene that maps to human chromosome 10q26.13. 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.

Gene ID: 80007