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Rabbit Anti-PEX14 Antibody (CSB-PA017800ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Peroxisomal membrane protein PEX14 Antibody,PTS1 receptor-docking protein Antibody,Peroxin-14 Antibody,Peroxisomal membrane anchor protein PEX14 Antibody,PEX14 AntibodyMore alternative names for the antibody
dJ734G22.2 antibody|NAPP2 antibody|NF E2 associated polypeptide 2 antibody|Peroxin 14 antibody|Peroxin-14 antibody|Peroxisomal biogenesis factor 14 antibody|Peroxisomal membrane anchor protein PEX14 antibody|Peroxisomal membrane anchor protein Pex14p antibody|Peroxisomal membrane protein PEX14 antibody|pex14 antibody|PEX14_HUMAN antibody|Pex14p antibody|PTS1 receptor docking protein antibody|PTS1 receptor-docking protein antibody
Anti-PEX14 antibody (ab109999)
Anti-PEX14 antibody (ab109999)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Peroxisomal membrane protein PEX14 protein (118-377AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:5195( Human), Entrez Gene:56273( Mouse), Entrez Gene:64460( Rat), Omim:601791( Human), SwissProt:O75381( Human), SwissProt:Q9R0A0( Mouse), SwissProt:Q642G4( Rat), Unigene:149983( Human), Unigene:184172( Mouse), Unigene:7844( Rat)
|Protein function|| |
Peroxisome membrane protein that is an essential component of the peroxisomal import machinery. Functions as a docking factor for the predominantly cytoplasmic PTS1 receptor (PEX5). Plays a key role for peroxisome movement through a direct interaction with tubulin. .
|Involvement in disease|| |
Peroxisome biogenesis disorder complementation group K (PBD-CGK) [MIM:614887]: A peroxisomal disorder arising from a failure of protein import into the peroxisomal membrane or matrix. The peroxisome biogenesis disorders (PBD group) are genetically heterogeneous with at least 14 distinct genetic groups as concluded from complementation studies. Include disorders are: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). ZWS, NALD and IRD are distinct from RCDP and constitute a clinical continuum of overlapping phenotypes known as the Zellweger spectrum (PBD-ZSS). . Note=The disease is caused by mutations affecting the gene represented in this entry.; Peroxisome biogenesis disorder 13A (PBD13A) [MIM:614887]: A fatal peroxisome biogenesis disorder belonging to the Zellweger disease spectrum and clinically characterized by severe neurologic dysfunction with profound psychomotor retardation, severe hypotonia and neonatal seizures, craniofacial abnormalities, liver dysfunction, and biochemically by the absence of peroxisomes. Additional features include cardiovascular and skeletal defects, renal cysts, ocular abnormalities, and hearing impairment. Most severely affected individuals with the classic form of the disease (classic Zellweger syndrome) die within the first year of life. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the peroxin-14 family.
|Protein cellular localization|| |
Peroxisome membrane ; Peripheral membrane protein ; Cytoplasmic side .
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CUSABIO BIOTECH CO.
|Product type|| |
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