PEX10 antibody (AA 1-100) (Biotin)

Catalog No. ABIN6982552

Product Details anti-PEX10 Antibody (Biotin)

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Binding Specificity: AA 1-100

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX10 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Cow

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human PEX10

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for PEX10

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Alternative Name: PEX10 (PEX10 Products)

Synonyms: ATPEX10 antibody, T9J22.2 antibody, peroxin 10 antibody, NALD antibody, PBD6A antibody, PBD6B antibody, RNF69 antibody, AV128229 antibody, Gm142 antibody, peroxin 10 antibody, peroxisomal biogenesis factor 10 antibody, PEX10 antibody, Pex10 antibody

Background:

Synonyms: AV128229, Gm142, MGC1998, NALD, OTTHUMP00000001658, PBD6A, PBD6B, peroxin 10, Peroxin-10, Peroxisomal biogenesis factor 10, Peroxisome assembly protein 10, Peroxisome biogenesis factor 10, PEX10, PEX10_HUMAN, RING finger protein 69, RNF69, RP23-298E4.1.

Background: This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Gene ID: 5192

UniProt: O60683

Pathways: Monocarboxylic Acid Catabolic Process