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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
Purified (azide-free) anti-β-Amyloid, 1-42
- 抗体英文名:
Purified (azide-free) anti-β-Amyloid, 1-42
- 供应商:
上海善然生物科技有限公司
- 保存条件:
2-8℃
- 规格:
1ml
Purified anti-β-Amyloid, 1-42 Antibody (Previously Covance catalog# SIG-39142)
12F4
Catalog# / Size
805503 / 1 mL
Clone
Regulatory Status RUO
Other Names AAA, ABETA, ABPP, AD1, APPI, CTFgamma, CVAP, PN-II, PN2, Amyloid beta A4 protein, preA4,
protease nexin-II, peptidase nexin-II, beta-amyloid peptide, alzheimer disease amyloid protein, cerebral
vascular amyloid peptide, APP, Amyloid Precursor Protein
Previously Signet Catalog# 9142-02
Signet Catalog# 9142-05
Signet Catalog# 9142-10
Covance Catalog# SIG-39142
Isotype Mouse IgG1, κ
Description Amyloid beta (Aβ or Abeta) denotes peptides of 36–43 amino acids in length that are crucially
involved in Alzheimer's disease as the main component of the amyloid plaques found in the brains of
Alzheimer patients. The peptides result from the amyloid precursor protein (APP), which is cut by
certain enzymes to yield Aβ. Aβ molecules can aggregate to form oligomers (known as "seeds")
which are believed to be able to induce other Aβ molecules to also take the misfolded oligomeric
form, leading to a chain reaction akin to a prion infection. The seeds or the resulting amyloid plaques
are toxic to nerve cells. The other protein implicated in Alzheimer's disease, tau protein, also forms
such prion-like misfolded oligomers, and there is some evidence that misfolded Aβ can induce tau to
misfold.
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文献和实验to the solubilizing power of the ionic detergents 16-BAC and SDS, respectively. Mitochondria were isolated from yeast cultures by differential centrifugation and were further purified by free flow electrophoresis (FFE) in zone-electrophoretic mode (ZE). Subsequently
alkyne?azide cycloaddition (CuAAC) reaction has been used to synthesize cyclic mini?DNA duplexes. The reaction is carried out on 5??alkyne?3??azide?labeled hairpin loop oligonucleotides and proceeds in high yield under mild conditions in as little as 5
Isolation of a Purified Epithelial Cell Population from Human Colon
While in situ techniques have been valuable in identifying the presence and localization of cytoplasmic and membrane components in tissue (1 ), there is often a need to study directly one or more cell types, free from its own microenvironment
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