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Details for Product No. ABIN264042

Prion Protein (PRNP) (AA 93-109) antibody

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ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30, AA960666, AI325101, PrP, PrPC, PrPSc, Prn-i, Prn-p, Sinc, prP27-30, prP33-35C, Prn, prp, Prp, SIP, PRPC, PRP, PRNP ... show more
»Alternatives AA 93-109
»Alternatives Cow (Bovine), Hamster, Human, Mouse (Murine), Sheep (Ovine)
»Alternatives Mouse
Clonality (Clone) Monoclonal ()
»Alternatives Un-conjugated
»Alternatives Immunohistochemistry (Frozen Sections) (IHC (fro)), ELISA, Western Blotting (WB)
Pubmed 4 references available
Catalog no. ABIN264042
Quantity 0.1 mL
1,160.50 $   Plus shipping costs $45.00
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Availability Will be delivered in 6 to 8 Business Days
Immunogen Full-length recombinant PrP
Clone 6D11
Isotype IgG2a
Characteristics Synonyms: Major prion protein, PrP27-30, PrP33-35C, ASCR, PRNP, PRIP
Purification Protein A Chromatography
Alternative Name CD230 / PrP
Background Prion protein PrP is a membrane glycosylphosphatidylinositol anchored glycoprotein thattends to aggregate into rod like structures. The encoded protein contains a highly unstableregion of five tandem octapeptide repeats. This gene is found on chromosome 20,approximately 20 kbp upstream of a gene which encodes a biochemically and structurallysimilar protein to the one encoded by this gene. Mutations in the repeat region as well aselsewhere in this gene have been associated with Creutzfeldt Jakob disease, fatal familialinsomnia, Gerstmann Straussler disease, Huntington disease like 1, and kuru. Twotranscript variants encoding the same protein have been found for this gene. All prion diseases share the same molecular pathogenic mechanism that involvesconversion of normal cellular prion protein (PrPc) into a form that is insoluble in non ionicdetergent and partially resistant to proteases (PrPsc). Both PrPsc and PrPc are encodedwithin a single exon of a chromosomal gene as a protein of ~ 250 amino acids. Manymammalian PrPs have a 22 amino acid N terminal signal sequence and 23 amino acid Cterminal signal sequence encoding for attachment of a glycosylphosphatidylinositolanchor. The mature protein of 209 amino acids contains one disulfide bond and has twosites of asparagine linked glycosylation.
UniProt P04156
Research Area CD Antigens, Surface Receptors of Immune Cells
Application Notes ELISA. Western blot. Immunohistochemistry: Epitope must be re-exposed in fixed tissues by pretreatment usingone of the following procedures: 1.70% Formic acid for 10-30 minutes at room temperature.2. Hydrolytic autoclavingOther applications not tested. Optimal dilutions are dependent on conditions and should be determined by the user.
Restrictions For Research Use only
Format Liquid
Concentration 2.0 mg/mL
Buffer PBS without preservatives
Preservative Without preservative
Storage -20 °C
Storage Comment Store the antibody at -20°C. Avoid repeated freezing and thawing. Do not store antibody diluted below 50?g/ml in the absence of protein (i. e. add 2% BSA). Shelf life: one year from despatch.
Expiry Date 12 months
Background publications Kascsak, Rubenstein, Merz et al.: "Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins." in: Journal of virology, Vol. 61, Issue 12, pp. 3688-93, 1987 (PubMed).

Kascsak, Tonna-DeMasi, Fersko et al.: "The role of antibodies to PrP in the diagnosis of transmissible spongiform encephalopathies." in: Developments in biological standardization, Vol. 80, pp. 141-51, 1994 (PubMed).

Kascsak, Fersko, Pulgiano et al.: "Immunodiagnosis of prion disease." in: Immunological investigations, Vol. 26, Issue 1-2, pp. 259-68, 1997 (PubMed).

Sigurdsson, Sy, Li et al.: "Anti-prion antibodies for prophylaxis following prion exposure in mice." in: Neuroscience letters, Vol. 336, Issue 3, pp. 185-7, 2002 (PubMed).

Alternatives for antigen "Prion Protein (PRNP)", type "Antibodies"
Hosts (70), (47), (20)
Reactivities (94), (64), (46), (36), (31), (4), (3), (3), (2), (1), (1), (1), (1), (1), (1), (1)
Applications (104), (80), (40), (39), (20), (15), (11), (9), (5), (4), (3), (3), (3)
Conjugates (3), (3), (2), (2), (2), (2), (2), (2), (2), (2), (2), (1)
Epitopes (21), (9), (6), (5), (4), (3), (3), (2), (1), (1), (1), (1), (1), (1)