Amyloid Beta Pyroglutamate 3-42 Pre-formed Fibrils

Human Amyloid Beta Pyroglutamate 3-42 Pre-formed Fibrils
Artikelnummer
STRSPR-492C
Verpackungseinheit
100 µg x2
Hersteller
Stressmarq Biosciences

Verfügbarkeit: wird geladen...
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Target: Amyloid Beta Pyroglutamate 3-42

Nature: Synthetic (TFA preparation, HFIP treated precursor)

Swiss-Prot: P05067

Biological Activity:

Expression System: N/A

Protein Length: 40 amino acids

Amino Acid Sequence: pyroEFRHDSGYEVHHQKLVFFAEDVGSNKGAIIGLMVGGVVIA

Purification: N/A

Purity: >95%

Storage Buffer: 10mM HCl with 2% DMSO

Protein Size: 4.3 kDa

Conjugate: No Tag

Cellular Localization: Cell Membrane,Intracellular Vesicles

Scientific Background: Our Amyloid Beta pyroglutamate 3-42 (pyro Aβ) Pre-formed Fibrils are generated from Amyloid Beta Peptide 3-42 pre-treated with 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP) using a previously published method (1,2). Our pyro Aβ3-42 fibrils present as primarily long strands when observed under TEM and AFM, and have a unique high molecular weight signal on a Western Blot with an anti-amyloid beta antibody.Amyloid beta peptide (Aβ) is generated by protease cleavage of amyloid precursor protein (APP), which aggregates into oligomers, protofibrils, fibrils and ultimately plaques. The accumulation of Aβ plaques in the brain is considered a hallmark of Alzheimer’s disease (AD), and most of the drugs tested for AD in the past 20 years have targeted amyloid beta accumulation (3). Pyroglutamate Aβ 3-42 is an N-terminally truncated peptide species that is modified by glutaminyl cyclase and has been reported to compromise 15-45% of total amyloid beta deposits in brains of AD patients (4,5). Pyroglutamate Aβ 3-42 exhibits higher aggregation propensity and neurotoxicity compared with full-length Aβ 1-42 (6,7) and is an active target in the next generation AD therapeutic development (8).

References: 1. Stine et al. 2003. JBC. 278(13):11612-22; doi: 10.1074/jbc.M2102072002. Chromy et al. 2003. Biochemistry. 42:12749-12760; doi: 10.1021/bi030029q3. Panza et al. 2019. Nat Rev Neurol. 15:73-88; https://doi.org/10.1038/s41582-018-0116-64. Valverde et al. 2021. JBC. 297:100963; https://doi.org/10.1016/j.jbc.2021.1009635.Schilling et al. 2008. Nat Med. 14:1106-11; DOI: 10.1038/nm.18726.Hartlage-Rubsamen et al. 2011. Acta Neuropathol. 121:705-19; 10.1007/s00401-011-0806-27.Xu, Wang and Wu. 2021. J Med Chem. 64:6549–65; DOI: 10.1021/acs.jmedchem.1c003258.Bayer. 2021. Nat Mol Psych. 27:1880-1885; https://doi.org/10.1038/s41380-021-01409-4

Field of Use: Not for use in humans. Not for use in diagnostics or therapeutics. For research use only.
Mehr Informationen
Artikelnummer STRSPR-492C
Hersteller Stressmarq Biosciences
Hersteller Artikelnummer SPR-492C
Green Labware Nein
Verpackungseinheit 100 µg x2
Mengeneinheit PAK
Reaktivität Human
Methode Western Blotting, In Vivo Assay, In Vitro Assay
Human Gene ID 351
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