HPS5 antibody

Catalog No. ABIN7228964

The Rabbit Polyclonal anti-HPS5 antibody has been validated for WB and ELISA. It is suitable to detect HPS5 in samples from Human and Mouse.

Quick Overview for HPS5 antibody (ABIN7228964)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HPS5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-HPS5 Antibody

Purpose: HPS5 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of HPS5 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

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

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: 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.

Target Details for HPS5

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

Alternative Name: HPS5

Background: Rabbit Anti-HPS5 Polyclonal Antibody,Hermansky-Pudlak syndrome 5 protein, Alpha-integrin-binding protein 63, Ruby-eye protein 2 homolog, Ru2,HPS5 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.,HPS5

Molecular Weight: observerd band 124kDa

Gene ID: 11234

UniProt: Q9UPZ3