PEX3 antibody

Catalog No. ABIN6571086

Product Details anti-PEX3 Antibody

Target: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX3 antibody is un-conjugated

Application: Immunohistochemistry (IHC)

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human PEX3 (NP_003621.1).

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for PEX3

Target: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Alternative Name: PEX3 (PEX3 Products)

Synonyms: DDBDRAFT_0204086 antibody, DDBDRAFT_0238047 antibody, DDB_0204086 antibody, DDB_0238047 antibody, zgc:56313 antibody, PBD10A antibody, TRG18 antibody, Peroxin-3 antibody, 1700014F15Rik antibody, 2810027F19Rik antibody, 2900010N04Rik antibody, peroxisomal biogenesis factor 3 antibody, peroxin 3 antibody, peroxisomal biogenesis factor 3 L homeolog antibody, LOC692959 antibody, CpipJ_CPIJ013204 antibody, pex3 antibody, PEX3 antibody, pex3.L antibody, Pex3 antibody

Background: The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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. Defects in this gene are a cause Zellweger syndrome (ZWS).

Molecular Weight:

Observed_MW: 37kDa

Calculated_MW: 42kDa

Gene ID: 8504

UniProt: P56589