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Merck
CN

A8978

Anti-Beta (β)-Amyloid antibody

mouse monoclonal, BAM90.1

别名:

抗-Aβ

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
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产品名称

抗-β-淀粉样蛋白 (13-28) 抗体,小鼠单克隆, clone BAM90.1, purified from hybridoma cell culture

biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

BAM90.1, monoclonal

form

buffered aqueous solution

species reactivity

human

packaging

antibody small pack of 25 μL

concentration

~2 mg/mL

technique(s)

enzyme immunoassay: 0.2-0.4 μg/mL using amyloid β-protein
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG1

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... APP(351)

Application

小鼠抗-β-淀粉样蛋白(13-28)单克隆抗体可用于免疫印迹分析(1:5,000 的稀释度)。该抗体还可用于IHC、免疫沉淀、荧光红外光谱和酶免疫测定(02-0.4μg/ml)。
成功使用该抗体的应用以及相关的同行评审论文如下所示。
免疫组织化学(1篇论文)

Disclaimer

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的人类或动物食用或应用。

General description

β-淀粉样蛋白前体蛋白 (APP) 是由蛋白水解酶β-分泌酶 (BACE1) 和 γ-分泌酶依次裂解,生成以Aβ1-42和 Aβ1-40型为主的β-淀粉样蛋白 (Aβ) 肽。分泌的Aβ肽通过再吸收机制和之后的内体降解过程降解,或通过胞外胰岛素降解酶降解。Aβ的胞外积累导致聚集体和原纤维的形成,最终形成淀粉样蛋白沉着物神经炎斑,其是阿尔茨海默病 (AD) 的标志物。
抗 β-淀粉样蛋白 [13-28] 单克隆抗体可识别β-淀粉样蛋白肽。抗体表位位于氨基酸 20-23 内。
淀粉样蛋白是由错误折叠的蛋白质和多肽组成的不溶性蛋白聚集体。淀粉样蛋白沉积与多种神经退行性疾病有关。

Physical form

在 0.01 M 磷酸盐缓冲盐水(pH 7.4)中过滤的溶液。

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存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

法规信息

常规特殊物品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Amyloid-beta-secondary structure distribution in cerebrospinal fluid and blood measured by an immuno-infrared-sensor: A biomarker candidate for Alzheimer?s disease
Nabers A, et al.
Analytical Chemistry, 88, 2755-2762 (2016)
Andreas Nabers et al.
EMBO molecular medicine, 10(5) (2018-04-08)
Alzheimer's disease (AD) is currently incurable, but there is general agreement that a minimally invasive blood biomarker for screening in preclinical stages would be crucial for future therapy. Diagnostic tools for detection of AD are either invasive like cerebrospinal fluid
Julia Stockmann et al.
Alzheimer's research & therapy, 12(1), 169-169 (2020-12-29)
We evaluated Aβ misfolding in combination with Aβ42/40 ratio as a prognostic tool for future clinical progression to mild cognitive impairment (MCI) or dementia due to Alzheimer's disease (AD) in individuals with subjective cognitive decline (SCD). Baseline plasma samples (n = 203)
Interactions of pathological hallmark proteins: Tubulin polymerization promoting protein/p25, beta-amyloid and alpha-synuclein
Olah J, et al.
The Journal of Biological Chemistry, jbc-M111 (2011)
Andreas Nabers et al.
Alzheimer's & dementia (Amsterdam, Netherlands), 11, 257-263 (2019-03-27)
Alzheimer's disease (AD) diagnosis requires invasive CSF analysis or expensive brain imaging. Therefore, a minimal-invasive reliable and cost-effective blood test is requested to power large clinical AD trials at reduced screening failure. We applied an immuno-infrared sensor to measure the

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