PRNP anticorps (C-Term)

N° du produit ABIN4889437

Cet anticorps Souris Monoclonal détecte spécifiquement PRNP dans WB, ELISA et IF. Il présente une réactivité envers Humain, Rat, Boeuf (Vache) et Mouton.

Aperçu rapide pour PRNP anticorps (C-Term) (ABIN4889437)

Antigène: PRNP (Prion Protein (PRNP))

Reactivité: Humain, Rat, Boeuf (Vache), Mouton

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp PRNP est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Clone: 4H7

Détail du produit anti-PRNP anticorps

Épitope: C-Term

Specificité: Reacts with full sequence PrP protein of brain tissue from different species (bovin, human, sheep, rat

Réactivité croisée: Mouton, Rat (Rattus)

Réactivité croisée (Details): .) Cross reacts with brain tissue from different species (bovin, human, sheep, rat ...)

Purification: Purified (protein A)

Immunogène: A 15 residue synthetic peptide derived from C-terminal domain of human PrP protein

Isotype: IgG2a kappa

Information d'application

Indications d'application:

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
IF(1:200 - 1:1000) WB(1:200 - 1:1000)

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Must be reconstituted in distilled water.

Concentration: 1 mg/mL

Buffer: Tris 0,1M, glycine 0,1M, sucrose 2 %

Stock: 4 °C/-20 °C

Stockage commentaire: 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.

Date de péremption: 24 months

Détails sur PRNP

Antigène: PRNP (Prion Protein (PRNP))

Autre désignation: Prion Protein (PrP)

Sujet: 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.

UniProt: P04156

Pathways: Transition Metal Ion Homeostasis, Activated T Cell Proliferation