GIDRP88 antibody

Catalog No. ABIN7243328

This Rabbit Polyclonal antibody specifically detects GIDRP88 in IHC and ELISA. It exhibits reactivity toward Human and Mouse.

Quick Overview for GIDRP88 antibody (ABIN7243328)

Target: GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GIDRP88 antibody is un-conjugated

Application: Immunohistochemistry (IHC), ELISA

Product Details anti-GIDRP88 Antibody

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Synthetic peptide of human R3HCC1L

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.7 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 GIDRP88

Target: GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))

Alternative Name: R3HCC1L

Background: C10orf28 (chromosome 10 open reading frame 28), also known as GIDRP88 (growth inhibition and differentiation-related protein 88) or putative mitochondrial space protein 32.1, is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, 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.

NCBI Accession: NP_001243548

UniProt: Q7Z5L2