PEX12 antibody (Center) (PE)

Catalog No. ABIN2793743

Product Details anti-PEX12 Antibody (PE)

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Binding Specificity: AA 131-158, Center

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX12 antibody is conjugated to PE

Application: Western Blotting (WB)

Purpose: Rabbit Anti-Human PEX12 (Center) Antibody

Immunogen: This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.

Isotype: Ig Fraction

Application Details

Application Notes: Western Blot
Recommended Dilutions
WB: 1:1000Western blot analysis of PEX12 Antibody (Center) was detected using the purified Pab.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Storage: 4 °C,-20 °C

Storage Comment: 2-8°C (short-term), -20°C (long-term)

Target Details for PEX12

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Alternative Name: PEX12 (PEX12 Products)

Synonyms: zgc:56182 antibody, pex12 antibody, MGC81372 antibody, PEX12 antibody, DDBDRAFT_0186545 antibody, DDBDRAFT_0238076 antibody, DDB_0186545 antibody, DDB_0238076 antibody, LOC100226224 antibody, PAF-3 antibody, PBD3A antibody, Peroxin-12 antibody, AI451906 antibody, peroxisomal biogenesis factor 12 antibody, peroxisomal biogenesis factor 12 L homeolog antibody, RING zinc finger-containing protein antibody, pex12 antibody, PEX12 antibody, pex12.L antibody, Pex12 antibody

Background:

Target Description: Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle.

Gene Symbol: PEX12

Molecular Weight: 40797 Da

Gene ID: 5193

UniProt: O00623