GIDRP88 anticorps

N° du produit ABIN7243328

Cet anticorps Lapin Polyclonal détecte spécifiquement GIDRP88 dans IHC et ELISA. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour GIDRP88 anticorps (ABIN7243328)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GIDRP88 est non-conjugé

Application: Immunohistochemistry (IHC), ELISA

Détail du produit anti-GIDRP88 anticorps

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Synthetic peptide of human R3HCC1L

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.7 mg/mL

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur GIDRP88

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

Autre désignation: R3HCC1L

Sujet: 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