β-Amyloid (1-12) Human DAEFRHDSGYEV-acid

  • Description

  • Application Data

Description

Amino acids 1-12 of the amyloid-beta peptide, a key subunit of extracellular plaques found in the brains of patients with Alzheimer’s disease

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Application Data

Catalogue number crb1000081
Molecular Weight 1424.43
Sequence (one letter code) DAEFRHDSGYEV-acid
Sequence (three letter code) H-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-OH
Molecular Weight 1424.43
Purity >95%
Storage - 20 ° C
References

Masters and Selkoe (2012) Biochemistry of Amyloid -Protein and Amyloid Deposits in Alzheimer Disease. Cold Spring Harb. Perspect. Med. 2(6) a006262 PMID: 22675658

 

Pearson Peers (2006) Physiological roles for amyloid β peptides. J. Physiol. 575(1) 5 PMID: 16809372

 

Selkoe and Hardy (2016) The amyloid hypothesis of Alzheimer's disease at 25 years. EMBO Mol. Med. 8(6) 595 PMID: 27025652

Data Sheet Material Safety Data Sheet (MSDS)

Amyloid β-peptide (Aβ) has been identified as the key subunit of the extracellular plaques found in the brains of patients with Alzheimer’s disease (AD) and Down’s syndrome (DS). Aβ has therefore been extensively studied as a potential target for treatment of AD.

Aβ is formed from the cleavage of the large, transmembrane protein; APP (amyloid precursor protein). Cleavage of APP by β- and then γ-secretases results in the formation of Aβ. Aβ can aggregate to produce amyloid-β oligomers, which are thought to be highly neurotoxic. Over time Aβ can further aggregate to produce the characteristic senile plaques present in AD and DS.

Aβ can be degraded by enzymes such as neprilysin, insulin degrading enzyme or endothelin converting enzyme. At physiological levels Aβ may be involved in controlling synaptic activity and neuronal survival.

β-Amyloid (1-12) Human

Cat No.Pack SizePriceQty.
1mg£110.00
0.5mg£85.00
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