跳转至内容
Merck
CN

GENXA931-1ML

Mouse IgG HRP Linked Whole Ab

Cytiva NXA931-1ML

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

NACRES:
NA.46
UNSPSC Code:
12352203
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


feature

wetted part: no

packaging

pkg of 1 mL

manufacturer/tradename

Cytiva NXA931-1ML

color

Colorless/brown (light)

storage temp.

2-8°C

General description

The antibodies are supplied with dilution guidelines for relevant applications and should be stored at 2° C to 8° C.

Features and Benefits

  • Highly species-specific.
  • Optimized for use with our range of ECL Detection Reagents.
  • Recommended dilutions to minimize background.

Analysis Note

To view the Certificate of Analysis for this product, please visit www.cytiva.com.

Legal Information

ECL is a trademark of Cytiva


pictograms

Exclamation mark

signalword

Warning

hcodes

存储类别

12 - Non Combustible Liquids

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



Liangzhi Sun et al.
Oncology letters, 20(3), 2447-2455 (2020-08-13)
Osteosarcoma (OS) is the most commonly diagnosed malignant cancer of bone that occurs in adolescents and children. Mounting number of studies have indicated that miRNAs are increasingly playing fundamental roles in OS development. Thus, the biological function of miR-429 in
Weixin Xie et al.
Journal of cellular and molecular medicine, 23(5), 3293-3301 (2019-02-19)
Recently, aberrant expression of miR-876-5p has been reported to participate in the progression of several human cancers. However, the expression and function of miR-876-5p in osteosarcoma (OS) are still unknown. Here, we found that the expression of miR-876-5p was significantly
Chen He et al.
Nature communications, 12(1), 4089-4089 (2021-07-04)
Pediatric high-grade glioma (pHGG) is a major contributor to cancer-related death in children. In vitro and in vivo disease models reflecting the intimate connection between developmental context and pathogenesis of pHGG are essential to advance understanding and identify therapeutic vulnerabilities.