PEX2 Antilichaam

This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein.

5828

P28328

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-130 of human PEX2 (NP_001165558.1) .

Unconjugated

Primary Antibodies

Signal Transduction

Affinity purification

LO2

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 35kDa

IgG

WB: 1:200 - 1:2000

PEX2

293T

HeLa

U-251MG

NIH/3T3

Mouse liver

Peroxisomal biogenesis factor 2

Homo sapiens

PXMP3, RNF72, RING finger protein 72, PMP35, PMP3, PEX2, peroxisome assembly factor-1, peroxisomal membrane protein 3, 35kDa, peroxin-2, peroxin 2, PAF-1, PAF1, PXMP3

WB

Liquid