HPS4 Antibody - BSA Free

Western Blot: HPS4 Antibody - BSA Free [NBP3-46084] - A375 cells were subjected to SDS PAGE followed by western blot with (HPS4 antibody) at dilution of 1:200

Immunoprecipitation: HPS4 Antibody - BSA Free [NBP3-46084] - IP result of anti-HPS4 ( for IP and Detection) with HeLa cell lysate.

Immunohistochemistry: HPS4 Antibody - BSA Free [NBP3-46084] - Immunohistochemistry of paraffin-embedded human liver tissue slide using (HPS4 Antibody) at dilution of 1:50

• Reactivity: Hu
• Applications: WB, ELISA, ICC/IF, IHC, IP
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free

HPS4 Antibody - BSA Free Summary

• Description: Novus Biologicals Rabbit HPS4 Antibody - BSA Free (NBP3-46084) is a polyclonal antibody validated for use in IHC, WB, ELISA, ICC/IF and IP. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Immunogen: Hermansky-Pudlak syndrome 4. (Uniprot# Q9NQG7)
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: HPS4
• Purity: Immunogen affinity purified

Applications/Dilutions

• Dilutions:
  • ELISA
  • Immunocytochemistry/ Immunofluorescence 1:20-1:200
  • Immunohistochemistry 1:20-1:200
  • Immunoprecipitation 1:200-1:1000
  • Western Blot 1:500-1:2000
• Theoretical MW: 70 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at -20C. Avoid freeze-thaw cycles.
• Buffer: PBS, 50% Glycerol, pH (7.3)
• Preservative: 0.02% Sodium Azide
• Purity: Immunogen affinity purified

Alternate Names for HPS4 Antibody - BSA Free

• bK1048E9.4
• Hermansky-Pudlak syndrome 4 protein
• Hermansky-Pudlak syndrome 4
• KIAA1667bK1048E9.5
• LE
• Light-ear protein homolog

Background

Hermansky-Pudlak syndrome is a disorder of organelle biogenesis in which oculocutaneous albinism, bleeding, and pulmonary fibrosis result from defects of melanosomes, platelet dense granules, and lysosomes. Mutations in this gene as well as several others can cause this syndrome. The protein encoded by this gene appears to be important in organelle biogenesis and is similar to the mouse 'light ear' protein. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]. Transcript Variant: This variant (1) encodes the longer isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: HPS4