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重要文件

MABN779

Sigma-Aldrich

Anti-Amyloid Beta 3NTyr10 Antibody, clone 4A5E8

clone 4A5E8, from mouse

同義詞:

Ab42, Amyloid beta 1-42, Abeta42, Abeta42(3NTyr10), Abeta42 (3NY10)

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

mouse

品質等級

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

4A5E8, monoclonal

物種活性

human

技術

ELISA: suitable
immunohistochemistry: suitable

同型

IgG2bκ

NCBI登錄號

運輸包裝

ambient

目標翻譯後修改

unmodified

基因資訊

human ... APP(351)

一般說明

Deposition of Amyloid beta (Ab) is an early event in the pathogenesis of Alzheimer s disease (AD). Ab peptides originate from the proteolytic cleavage of the amyloid precursor protein (APP). The beta-secretase cleaves APP between residues Met671 and Asp672 and yields sAPP beta and C99. Following the beta-secretase cleavage, a second cleavage occurs at the C-terminus of Ab peptide that releases Ab from C99. This cleavage occurs in the vicinity of residue 712 of the C-terminus. The gamma-secretase can cleave the C-terminal region at either Val711 or Ile713 to produce the shorter Ab peptide (Ab1-40) or the longer Ab peptide (Ab1-42). Ab1-42 occurs more frequently and forms fibrillar aggregates far more readily than the Ab1-40 peptide. In AD, upregulation of inducible nitric oxide synthase (NOS2), results in tyrosine nitration of several proteins, including Ab, which accelerates its aggregation. APP/PS1/Nlrp3 mice display less nitrated Ab and a reduced average plaque size as well as fewer nitrated plaque cores. NOS2 deficiency and treatment with NOS2 inhibitors is shown to reduce 3NTyr (10)-Ab and overall Ab deposition and cognitive dysfunction in APP/PS1 mice. Also, injection of 3NTyr(10)-A into the brain of young APP/PS1 mice leads to induction of beta-amyloidosis. (Ref.: Heneka, MT et al (2013). Nature 493, 674-678; Kummer, MP et al (2011). Neuron. 71(5):833-844).

特異性

Clone 4A5E8 detects amyloid beta 1-42 nitrated at position 10 in human.

免疫原

Synthetically nitrated linear peptide corresponding to 12 amino acids in the beta amyloid beta 1-42 peptide.

應用

Anti-Amyloid Beta 3NTyr10 Antibody, clone 4A5E8, Cat. No. MABN779, is a highly specific mouse monoclonal antibody that targets 3NTyr10 and has been tested in ELISA and Immunohistochemistry.
ELISA Analysis: A representative lot detected Amyloid Beta 3NTyr10 in ELISA applications (Heneka, M.T., et. al. (2013). Nature. 493(7434):674-8).

Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected Amyloid Beta 3NTyr10 in unfixed cortical brain sections from a control verses clinically confirmed AD (Braak stage V) cases. (Courtesy of Dr. Markus Kummer and Prof. Dr. Michael Heneka, MD, University of Bonn, Department of Neurology, Clinical Neurosciences, Germany).
Research Category
Neuroscience

品質

Isotype testing: Identity Confirmation by Isotyping Test.

Isotyping Analysis: The identity of this monoclonal antibody is confirmed by isotyping test to be mouse IgG2b .

標靶描述

~4.51 kDa calculated. Beta amyloid peptides aggregate in Alzheimer′s disease brain.

外觀

Protein G purified
Format: Purified
Purified mouse monoclonal antibody IgG2b in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

儲存和穩定性

Stable for 1 year at 2-8°C from date of receipt.

其他說明

Concentration: Please refer to lot specific datasheet.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 2


分析證明 (COA)

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Reem A Mohamed et al.
Molecules (Basel, Switzerland), 26(16) (2021-08-28)
Since westernized diet-induced insulin resistance is a risk factor in Alzheimer's disease (AD) development, and lipopolysaccharide (LPS) coexists with amyloid β (Aβ)1-42 in these patients, our AD novel model was developed to resemble sporadic AD by injecting LPS into high

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