PEX10 antibody (AA 1-100) (Cy5)

Catalog No. ABIN6984029

The Rabbit Polyclonal anti-PEX10 antibody has been validated for IF (cc) and IF (p). It is suitable to detect PEX10 in samples from Mouse.

Quick Overview for PEX10 antibody (AA 1-100) (Cy5) (ABIN6984029)

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

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX10 antibody is conjugated to Cy5

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-PEX10 Antibody (Cy5)

Binding Specificity: AA 1-100

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for PEX10

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

Alternative Name: PEX10

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