PEX13 antibody (C-Term)

Catalog No. ABIN2856329

The Rabbit Polyclonal anti-PEX13 antibody has been validated for WB and IHC (p). It is suitable to detect PEX13 in samples from Human.

Quick Overview for PEX13 antibody (C-Term) (ABIN2856329)

Target: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX13 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-PEX13 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human

Characteristics: Rabbit polyclonal antibody to PEX13 (peroxisome biogenesis factor 13)
PEX13 antibody [C3], C-term

Purification: Purified by antigen-affinity chromatography.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human PEX13. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: Molt-4

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for PEX13

Target: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Alternative Name: peroxisomal biogenesis factor 13

Background: This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.

Cellular Localization: Peroxisome membrane, Single-pass membrane protein

Molecular Weight: 44 kDa

Gene ID: 5194

UniProt: Q92968

Pathways: Feeding Behaviour, Monocarboxylic Acid Catabolic Process