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Merck
CN

AEC101

Sigma-Aldrich

AEC 染色试剂盒

liquid

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别名:
ACE substrate kit
UNSPSC代码:
41116134
NACRES:
NA.32

形式

liquid

质量水平

用途

sufficient for ≥1,000 tests (150 ml substrate solution)

储存温度

2-8°C

相关类别

应用

AEC染色试剂盒作为底物用于:
  • 通过组织学和免疫组化法在细胞种子基质切片中培养出ExtrAvidin过氧化物酶抗体
  • 体外酶联免疫斑点(ELISPOT)分析中外周血单核细胞中的链霉亲和素-辣根过氧化物酶
  • 附睾脂肪垫免疫组织染色中的小鼠IgG生物素化二次抗体

包装

本试剂盒包含3mL的浓缩醋酸盐缓冲液、3-amino-9-ethylcarbazole (AEC) 显色剂及过氧化氢,采用滴瓶包装,滴加方便。附带各种应用的使用说明。

注意

在2-8 °C下至少可稳定保存1年。

相关产品

产品编号
说明
价格

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 1B

WGK

WGK 3

闪点(°F)

134.6 °F

闪点(°C)

57 °C

法规信息

危险化学品

分析证书(COA)

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Leeann T Blalock et al.
Oncoimmunology, 1(3), 287-357 (2012-06-28)
Dendritic cell (DC) immunotherapy has shown a promising ability to promote anti-tumor immunity in vitro and in vivo. Many trials have tested single epitopes and single antigens to activate single T cell specificities, and often CD8(+) T cells only. We
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Vincenti D, et al.
Molecular Medicine, 9(3), 105-105 (2003)
Uncoupling of inflammation and insulin resistance by NF-kappaB in transgenic mice through elevated energy expenditure
Tang T, et al.
Test, 285(7), 4637-4644 (2010)
Leslie R Morse et al.
Translational stroke research, 2(4), 643-650 (2012-03-01)
Spinal cord injury is associated with rapid bone loss and arrested long bone growth due to mechanisms that are poorly understood. In this study, we sought to determine the effects of severe T10 contusion spinal cord injury on the sublesional
Kuangda Lu et al.
Journal of the American Chemical Society, 138(38), 12502-12510 (2016-08-31)
Photodynamic therapy (PDT) can destroy local tumors and minimize normal tissue damage, but is ineffective at eliminating metastases. Checkpoint blockade immunotherapy has enjoyed recent success in the clinic, but only elicits limited rates of systemic antitumor response for most cancers

实验方案

本实验方案通过对石蜡包埋的组织切片中的特定抗原进行染色和成像,完成整个免疫组织化学(IHC)操作步骤。

Use this protocol to for the entire immunohistochemistry (IHC) procedure through staining and visualization of specific antigens in paraffin-embedded tissue sections.

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