PEX16 antibody (N-Term)

Catalog No. ABIN8020749

The Rabbit Polyclonal anti-PEX16 antibody is suitable to detect PEX16 in samples from Human, Mouse and Rat. It has been validated for WB, IF, ICC and IP.

Quick Overview for PEX16 antibody (N-Term) (ABIN8020749)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX16 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunoprecipitation (IP)

Product Details anti-PEX16 Antibody

Binding Specificity: N-Term

Purpose: Anti-PEX16 Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Predicted Reactivity: Human PEX16 shares 94.4% amino acid (aa) sequence identity with mouse PEX16.

Characteristics: Anti-PEX16 Antibody. Tested in WB, ICC, IF, IP applications. This antibody reacts with Human, Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the N-terminus of human PEX16. Human PEX16 shares 94.4% amino acid (aa) sequence identity with mouse PEX16.

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human Immunoprecipitation, 0.5-2 μg/mL, Human

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for PEX16

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

Alternative Name: PEX16

Background:

Background: The protein encoded by this gene 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 this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described

Gene Full Name: peroxisomal biogenesis factor 16

Molecular Weight: 42 kDa

Gene ID: 9409

UniProt: Q9Y5Y5