PEX12 antibody (AA 131-158)

Catalog No. ABIN653557

Product Details anti-PEX12 Antibody

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

Binding Specificity: AA 131-158

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX12 antibody is un-conjugated

Application: Western Blotting (WB)

Predicted Reactivity: B, M

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

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.

Clone: RB22647

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

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: 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.

Molecular Weight: 40797

Gene ID: 5193

NCBI Accession: NP_000277

UniProt: O00623