HPS5 anticorps

N° du produit ABIN7228964

L’anticorps anti-HPS5 Polyclonal Lapin est utilisé pour la détection de HPS5 dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour HPS5 anticorps (ABIN7228964)

Antigène: HPS5 (Hermansky-Pudlak Syndrome 5 (HPS5))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HPS5 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-HPS5 anticorps

Fonction: Rabbit Anti-HPS5 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of HPS5 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human HPS5 protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur HPS5

Antigène: HPS5 (Hermansky-Pudlak Syndrome 5 (HPS5))

Autre désignation: HPS5

Sujet: Hermansky-Pudlak syndrome 5 protein, Alpha-integrin-binding protein 63, Ruby-eye protein 2 homolog, Ru2HPS5 encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of integrin, alpha-3. Mutations in HPS5 are associated with Hermansky-Pudlak syndrome type 5. Multiple transcript variants encoding two distinct isoforms have been identified for HPS5. HPS5 (HPS5, Biogenesis Of Lysosomal Organelles Complex 2 Subunit 2) is a Protein Coding gene. Diseases associated with HPS5 include Hermansky-Pudlak Syndrome 5 and Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis. An important paralog of HPS5 is TECPR2.

Poids moléculaire: 124kD

ID gène: 11234

UniProt: Q9UPZ3