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Merck
CN

06-225

抗-c-Jun抗体

serum, Upstate®

别名:

Activator protein 1, AP1, p39, Proto-oncogene c-Jun, Transcription factor AP-1, V-jun avian sarcoma virus 17 oncogene homolog

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
immunocytochemistry
immunoprecipitation (IP)
western blot
Species reactivity:
human, avian, mouse
Citations:
23
Technique(s):
immunocytochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
Uniprot accession no.:
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产品名称

抗-c-Jun抗体, serum, Upstate®

biological source

rabbit

conjugate

unconjugated

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human, avian, mouse

manufacturer/tradename

Upstate®

technique(s)

immunocytochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... JUN(3725)
mouse ... Jun(16476)

Analysis Note

对照
阳性抗原对照:目录# 12-303,Jurkat细胞裂解液。
已通过免疫印迹对人A431细胞或Jurkat细胞裂解液的RIPA裂解液进行了常规评估

Application

用抗c-Jun兔多克隆抗血清(目录号06-225)检测c-Jun(又称转录因子AP-1),已被证明可用于免疫细胞化学,免疫沉淀和蛋白质印迹。
研究子类别
转录因子
研究类别
表观遗传学&核功能

Biochem/physiol Actions

c-Jun

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消费或应用于人类或动物。

General description

35-39 kDa
c-Jun是转录因子AP-1的一部分,可结合并激活TRE/AP-1元件上的转录,并且似乎是SAPK/JNK信号通路的主要下游靶标。c-Jun的转录活性受Ser63和Ser73的磷酸化的调节。胞外信号(包括生长因子、转化癌蛋白和紫外线照射)刺激c-Jun在Ser63/73处的磷酸化并激活c-Jun依赖性转录。Ser63/73的突变使c-Jun对有丝分裂和应激诱导的
信号通路无反应。MAP激酶的同系物,SAPK/JNK,与c-Jun的N端结合,并在Ser63/73处磷酸化c-Jun。此外,激活c-Jun的信号同样也刺激SAPK/JNK的活性。

Immunogen

含有禽c-Jun DNA结合域的Trp E融合蛋白

Other Notes

替代:04-210

Physical form

全兔抗血清,含0.05%叠氮化钠
抗血清

Preparation Note

在-20°C下可保存2年

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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存储类别

10 - Combustible liquids

wgk

WGK 1


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Multiple mitogen-activated protein kinases are regulated by hyperosmolality in mouse IMCD cells.
T Berl, G Siriwardana, L Ao, L M Butterfield, L E Heasley, T Berl, G Siriwardana, L Ao et al.
The American Journal of Physiology null
Characterization of the chromosomal binding sites and dimerization partners of the viral oncoprotein Meq in Marek's disease virus-transformed T cells.
Alon M Levy, Yoshihiro Izumiya, Peter Brunovskis, Liang Xia, Mark S Parcells et al.
Journal of virology null
The oncogenic microRNA OncomiR-21 overexpressed during Marek's disease lymphomagenesis is transactivated by the viral oncoprotein Meq.
Stik, G; Dambrine, G; Pfeffer, S; Rasschaert, D
Journal of virology null
Myristylation alters DNA-binding activity and transactivation of FBR (gag-fos) protein
Kamata, N., et al
Molecular and cellular biology, 11, 765-772 (1991)
Steffen Klippel et al.
British journal of haematology, 159(3), 340-351 (2012-09-14)
Jasmonates, plant stress hormones, have been demonstrated to be effective in killing various types of cancer cells. We therefore tested if methyljasmonate (MJ) has activity against multiple myeloma (MM) in vitro and in vivo. MM cell lines and primary MM

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