跳转至内容
Merck
CN

ABE1948

Anti-CLIM-1/2 Antibody

serum, from rabbit

别名:

LIM domain-binding protein 2, LDB-2, Carboxyl-terminal LIM domain-binding protein 1, CLIM-1, LIM domain-binding factor CLIM1, CLIM-1/2

登录 查看组织和合同定价。

选择尺寸


关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
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
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

产品名称

Anti-CLIM-1/2 Antibody, serum, from rabbit

biological source

rabbit

conjugate

unconjugated

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

chicken, hamster, human, mouse

technique(s)

ChIP: suitable
immunocytochemistry: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... LDB2(9079)

Analysis Note

Evaluated by Western Blotting in E16 embryonic mouse brain tissue lysate.

Western Blotting Analysis: A 1:5,000 dilution of this antibody detected CLIM-1/2 in 10 µg of E16 embryonic mouse brain tissue lysate.

Application

This Anti-CLIM-1/2 Antibody is validated for use in Western Blotting, Immunocytochemistry, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry, Immunofluorescence for the detection of CLIM-1/2.
Western Blotting Analysis: A representative lots detected endogenous CLIM1/2 in CHO and murine pituitary gonadotroph Alpha T3 cells, as well as bacterially expressed and in vitro tranlsated recombinant CLIM1/2 (Ostendorff, H.P., et al. (2006). Dev Dyn. 235(3):786-791; Ostendorff, H.P., et al. (2002). Nature. 416(6876):99-103).
Immunocytochemistry Analysis: A representative lot revealed an inverse correlation between the expression level of endogenous CLIM1/2 and that of its negative regulator RLIM in HEK293, CHO, murine pituitary gonadotroph Alpha T3, and chicken ectodermal cells by dual fluorescent immunocytochemistry (Ostendorff, H.P., et al. (2002). Nature. 416(6876):99-103).
Chromatin Immunoprecipitation (ChIP) Analysis: A representative lot detected CLIM1/2 occupancy at the alphaGSU promoter in murine pituitary gonadotroph Alpha T3 cells (Ostendorff, H.P., et al. (2002). Nature. 416(6876):99-103).
Immunohistochemistry Analysis: A representative lot detected similar stage-dependent expression patterns between CLIM1/2 and the ubiquitin ligase RLIM in the developing neural tube during early mouse embryogenesis (Ostendorff, H.P., et al. (2006). Dev Dyn. 235(3):786-791).
Immunofluorescence Analysis: A representative lot revealed highly co-localized expressions of CLIM1/2 and RLIM on thoracic sections from E12.5 mouse embryos by dual fluorescent immunohistochemistry (Ostendorff, H.P., et al. (2006). Dev Dyn. 235(3):786-791).

Biochem/physiol Actions

Reacts with both CLIM1 and CLIM2. Expected to react with all spliced isoforms of CLIM1 (CLIM-1a, CLIM-1b, and isoform 3) & CLIM2 (Visvader-a, Tran-a, Tran-b).

General description

LIM domain-binding protein 1 (UniProt P70662; CLIM-2, LDB-1) encoded by the murine Ldb2 gene (Clim2, Nli; Gene ID 16825) and LIM domain-binding protein 2 (UniProt O55203; CLIM-1, LDB-2, CLP-36) encoded by the murine Ldb2 gene (Clim1; Gene ID 16826) are LIM domain-interacting cofactors whose interaction with LIM homeodomain (LIM-HD) transcription factors are crucial for the development of specific types of interneurons and motor neurons during neural tube development. The ubiquitin ligase RLIM targets CLIM for proteasomal degradation, thereby inhibiting developmental LIM-HD activity.
~50/43 kDa observed. Uncharacterized band(s) may appear in some lysates.

Immunogen

Recombinant protein corresponding to mouse CLIM-1.

Other Notes

Concentration: Please refer to lot specific datasheet.

未找到合适的产品?  

试试我们的产品选型工具.

存储类别

10 - Combustible liquids

wgk

WGK 1


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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

相关内容

A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持