Quimigen Portugal > Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), HRP conjugated
Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), HRP conjugated
Referencia TA501430BM
embalaje : 100ul
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PEX5 Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI6E9]
SKU
TA501430BM
Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), HRP conjugated
| Product Data | |
| Clone Name | OTI6E9 |
|---|---|
| Application | FC, IF, WB |
| Recommended Dilution | WB 1:500~2000, IF 1:100, FLOW 1:100 |
| Reactivity | Dog, Human, Monkey, Mouse, Rat |
| Antibody Host | Mouse |
| Isotype | IgG1 |
| Clonality | Monoclonal |
| Immunogen | Full length human recombinant protein of human PEX5 (NP_000310) produced in HEK293T cell. |
| Buffer | PBS (pH 7.3) containing 1% BSA, 50% glycerol. |
| Concentration | 0.5 mg/ml |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | HRP |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Shipping | Blue Ice |
| Predicted Protein Size | 69.7 kDa |
| Gene Name | peroxisomal biogenesis factor 5 |
| Database Link | |
| Background | The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq] |
| Synonyms | PBD2A; PBD2B; PTS1-BP; PTS1R; PXR1; RCDP5 |
| Reference Data | |
| Protein Families | Druggable Genome |
| Product Manuals |
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| SDS |
| Antibody Resources |
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| SKU | Description | Size | ||
|---|---|---|---|---|
| CF501430 | Carrier-free (BSA/glycerol-free) PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9) | 100 ug | | |
| TA501430 | Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9) | 100 ul | | |
| TA501430AM | Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), Biotinylated | 100 ul | | |
| TA501430S | Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9) | 30 ul | | |