Amyloid Precursor Protein (APP) Rabbit Polyclonal Antibody
Other products for "APP"
Specifications
| Product Data | |
| Applications | WB |
| Recommended Dilution | IHC: 1:1000-1:10000, IP: 1:1000 |
| Reactivities | Human, Mouse, Rat, Eukaryotes |
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | Synthetic molecular mimic of soluble oligomers. |
| Formulation | PBS, 50% glycerol, 0.09% sodium azide |
| Concentration | lot specific |
| Purification | Protein A Purified |
| Conjugation | Unconjugated |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Gene Name | amyloid beta precursor protein |
| Database Link | |
| Background | Amyloid monomeric proteins can sometimes oligomerize into destructive amyloid fibrils.Amyloidogenic conformations of non-disease related proteins can be created by partial protein misfolding or denaturation. Many degenerative diseases are known to be related to the accumulation of misfolded proteins as amyloid fibres . These include the amyloid- peptide plaques and tau neurofibrillary tangles in senile plaques of Alzheimers symptomology, the deposition of -synuclein in the Lewy bodies of Parkinsons disease, and accumulation of polyglutamine-containing aggregates in Huntingtons disease . |
| Synonyms | AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2 |
| Note | Recognizes all types of amyloid oligomers. Appears to recognize a peptide backbone epitope that is common to amyloid oligomers, but is not found in native proteins, amyloidogenic monomer or mature amyloid fibrils. |
| Reference Data | |
| Protein Families | Druggable Genome, Transmembrane |
| Protein Pathways | Alzheimer's disease |
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