PEX16 Monoclonal antibody, PBS Only
PEX16 Monoclonal Antibody for WB, Indirect ELISA
Host / Isotype
Mouse / IgG1
Reactivity
Human, Rat, Mouse
Applications
WB, Indirect ELISA
Conjugate
Unconjugated
CloneNo.
2D7G4
验证数据展示
产品信息
68261-1-PBS targets PEX16 in WB, Indirect ELISA applications and shows reactivity with Human, Rat, Mouse samples.
| Tested Applications | WB, Indirect ELISA Application Description |
| Tested Reactivity | Human, Rat, Mouse |
| Immunogen | PEX16 fusion protein Ag6574 种属同源性预测 |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Full Name | peroxisomal biogenesis factor 16 |
| Synonyms | Peroxin 16, PEX16 |
| Calculated Molecular Weight | 39 kDa |
| Observed Molecular Weight | 38 kDa |
| GenBank Accession Number | BC000467 |
| Gene Symbol | PEX16 |
| Gene ID (NCBI) | 9409 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Protein G purification |
| UNIPROT ID | Q9Y5Y5 |
| Storage Buffer | PBS Only |
| Storage Conditions | Store at -80°C. The product is shipped with ice packs. Upon receipt, store it immediately at -80°C |
背景介绍
Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. Peroxin 16, also known as PEX16 or Peroxisomal biogenesis factor 16, is a 336 amino acid integral membrane protein that has a critical role in the biogenesis of peroxisomes. PEX16 together with PEX3 and PEX19 are specifically involved in peroxisomal membrane protein (PMP) import. Defects in the gene encoding Peroxin 16 are the cause of multiple peroxisome-related disorders, including Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), classical rhizomelic chondrodysplasia punctata (RCDP) and peroxisome biogenesis disorder complementation group 9 (PBD-CG9).