PEX16 antibody (AA 100-180)

Catalog No. ABIN7230596

The Rabbit Polyclonal anti-PEX16 antibody (ABIN7230596) specifically detects PEX16 in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for PEX16 antibody (AA 100-180) (ABIN7230596)

Target: PEX16 (Peroxisomal Biogenesis Factor 16 (PEX16))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX16 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-PEX16 Antibody

Binding Specificity: AA 100-180

Purpose: Rabbit Anti-PEX16 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of PEX16 protein

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

Immunogen: Synthesized peptide derived from part region of human PEX16 protein at AA range: 100-180

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: ProClin

Precaution of Use: This product contains ProClin: 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.

Expiry Date: 12 months

Target Details for PEX16

Target: PEX16 (Peroxisomal Biogenesis Factor 16 (PEX16))

Alternative Name: PEX16

Background: Peroxisomal membrane protein PEX16, Peroxin-16, Peroxisomal biogenesis factor 16PEX16 (Peroxisomal Biogenesis Factor 16) is a Protein Coding gene. Diseases associated with PEX16 include Peroxisome Biogenesis Disorder 8B and Peroxisome Biogenesis Disorder 8A. Among its related pathways are Peroxisome. The protein encoded by PEX16 is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of PEX16 product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for PEX16 and two variants have been described.

Molecular Weight: 36kD

Gene ID: 9409

UniProt: Q9Y5Y5