PEX13 antibody (AA 342-403)

Catalog No. ABIN1886384

Product Details anti-PEX13 Antibody

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

Binding Specificity: AA 342-403

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX13 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: Purified by antigen-affinity chromatography.

Immunogen: Synthetic peptide contain a sequence corresponding to a region within amino acids 342 and 403 of Human PEX13

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for PEX13

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

Alternative Name: Peroxin 13 (PEX13 Products)

Synonyms: CG4663 antibody, DmelPex13 antibody, Dmel\\CG4663 antibody, pex13 antibody, zgc:66124 antibody, PAS20 antibody, DDBDRAFT_0191662 antibody, DDBDRAFT_0238077 antibody, DDB_0191662 antibody, DDB_0238077 antibody, NALD antibody, PBD11A antibody, PBD11B antibody, ZWS antibody, 2610008O20Rik antibody, Peroxin 13 antibody, peroxisomal biogenesis factor 13 antibody, peroxin PEX13 antibody, peroxin 13 (predicted) antibody, peroxin antibody, SH3 domain-containing protein antibody, putative peroxin 13 antibody, peroxisome biogenesis factor 13 antibody, Pex13 antibody, pex13 antibody, PEX13 antibody

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.[provided by RefSeq]

Molecular Weight: 44 kDa

Gene ID: 5194

NCBI Accession: NM_002618, NP_002609

Pathways: Feeding Behaviour, Monocarboxylic Acid Catabolic Process