Peroxin 2 (V14) Peptide

Peroxins are proteins involved in peroxisome biogenesis The peroxisome biogenesis factor Peroxin 2 (also designated Pex2) is an integral membrane protein of peroxisomes. Defects in the PXMP3 gene encoding Peroxin 2 are the cause of Zellweger syndrome-1 (ZWS-1), an autosomal recessive disorder due to defective import mechanisms for peroxisomal matrix enzymes. ZWS-1 is a severe form of the peroxisome-biogenesis disorders, a group of genetically heterogeneous, lethal diseases that are characterized by neuronal, hepatic and renal abnormalities, mental retardation and, in their most severe form, death within the first year of life.

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SPECIFICATIONS

Catalog Number

BS3900P

Applications

BNI

Form

1 mg/ml in DI water.

Purity

Synthetic peptide Peroxin 2 (V14). (Note: the amino acid sequence is proprietary). The purity is > 98%.

Swiss Prot

P28328

Storage Temp

Store at 4 degree C short term. Aliquot and store at -20 degree C long term. Avoid freeze-thaw cycles.

Additional Info

This peptide can be used with studies using BS3900 Peroxin 2 (V14) pAb.

Alternative Names

35 kDa peroxisomal membrane protein; PAF-1; PAF1; Peroxin-2; peroxisomal biogenesis factor 2; Peroxisomal membrane protein 3; peroxisomal membrane protein 3; 35kDa; peroxisome assembly factor 1; Peroxisome biogenesis factor 2; PEX2; PEX2; PMP3; PMP35; PXMP3; RING finger protein 72; RNF72; ZWS3