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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
$306.10
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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