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Prion Protein PrP antibody (4H7)
Major prion protein
ASCR
PrP27-30
PrP33-35C
CD230
Gene name : PRNP, PRIP, PRP
ASCR
PrP27-30
PrP33-35C
CD230
Gene name : PRNP, PRIP, PRP
As low as
€278.30
In stock
Ref
00012734
PrP is found in high quantity in the brain of humans and animals infected with neurodegenerative diseases known as transmissible spongiform encephalopathies or prion diseases, like: Creutzfeldt-Jakob disease (CJD), fatal familial insomnia (FFI), Gerstmann-Straussler disease (GSD), Huntington disease-like type 1 (HDL1) and kuru in humans; scrapie in sheep and goat; bovine spongiform encephalopathy (BSE) in cattle.
| ID Covalab | mab0026-P |
|---|---|
| Product type | Primary antibodies |
| Clonality | Monoclonal antibody |
| Clone | 4H7 |
| Isotype | IgG2a / Kappa |
| Raised in | Mouse |
| Immunogen | A 15 residue synthetic peptide derived from C-terminal domain of human PrP protein |
| Activity cross reaction | Reacts with full sequence PrP protein of brain tissue from different species (bovin, human, sheep, rat ..) Cross reacts with brain tissue from different species (bovin, human, sheep, rat …) |
| Species | Bov, Hu, Rat, Sh |
| Labelling | None |
| Form | Purified (protein A) |
| Preservative | None |
| Storage instructions | Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt. |
| Target | Prion Protein (PrP) |
| Uniprot ID | P04156 |
| Applications | ELISA, IF, WB |
| Working dilutions | Optimal dilution should be determined by the end user. The following are guidelines only : IF (1:200 - 1:1000) WB (1:200 - 1:1000) |
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