GIDRP88 Antikörper

Produktnummer ABIN7243328

Produktdetails anti-GIDRP88 Antikörper

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GIDRP88 Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC), ELISA

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Synthetic peptide of human R3HCC1L

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.7 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

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

Details zu GIDRP88

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

Andere Bezeichnung: R3HCC1L (C10orf28 Produkte)

Synonyme: 1700036B12Rik antikoerper, AI450607 antikoerper, C10orf28 antikoerper, D19Ertd386e antikoerper, GIDRP86 antikoerper, Gidrp88 antikoerper, GIDRP88 antikoerper, PSORT antikoerper, R3H domain and coiled-coil containing 1 like antikoerper, R3hcc1l antikoerper, R3HCC1L antikoerper

Hintergrund: 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