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Merck
所有图片(1)

文件

19-147

Sigma-Aldrich

U0126

solid, suitable for kinase activity assay

别名:

Kinase inhibitor, MEK inhibitor

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About This Item

分類程式碼代碼:
12352200
eCl@ss:
32160405
NACRES:
NA.41

product name

U0126, U0126 is a elective inhibitor of MEK-1 and MEK-2; weak inhibitor of PKC, Raf, ERK, JNK, MEKK, MKK-3, MKK-4/SEK, MKK-6, Abl, Cdk2 and Cdk4.

品質等級

形狀

solid

製造商/商標名

Upstate®

技術

activity assay: suitable (kinase)

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

基因資訊

human ... MAP2K1(5604)

生化/生理作用

抑制剂种类:激酶
蛋白质靶标:MAPKK 1

外觀

C18H16N6S2

儲存和穩定性

在-20°C下可保存2年

法律資訊

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

免責聲明

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。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Inhibition of MAP kinase kinase prevents cytokine and prostaglandin E2 production in lipopolysaccharide-stimulated monocytes.
Scherle, P A, et al.
Journal of immunology (Baltimore, Md. : 1950), 161, 5681-5686 (1998)
Jahangir Iqbal et al.
The Journal of biological chemistry, 295(13), 4101-4113 (2020-02-13)
The hormone leptin regulates fat storage and metabolism by signaling through the brain and peripheral tissues. Lipids delivered to peripheral tissues originate mostly from the intestine and liver via synthesis and secretion of apolipoprotein B (apoB)-containing lipoproteins. An intracellular chaperone
D R DeSilva et al.
Journal of immunology (Baltimore, Md. : 1950), 160(9), 4175-4181 (1998-05-09)
Three mitogen-activated protein kinase pathways are up-regulated during the activation of T lymphocytes, the extracellular signal-regulated kinase (ERK), Jun NH2-terminal kinase, and p38 mitogen-activated protein kinase pathways. To examine the effects of blocking the ERK pathway on T cell activation
Jewon Jung et al.
iScience, 24(7), 102701-102701 (2021-07-06)
Inhibition of TRPML1, which is encoded by MCOLN1, is known to deter cell proliferation in various malignancies. Here, we report that the tumor suppressor, p53, represses MCOLN1 in the urothelium such that either the constitutive loss or ectopic knockdown of
M F Favata et al.
The Journal of biological chemistry, 273(29), 18623-18632 (1998-07-11)
The compound U0126 (1,4-diamino-2,3-dicyano-1, 4-bis[2-aminophenylthio]butadiene) was identified as an inhibitor of AP-1 transactivation in a cell-based reporter assay. U0126 was also shown to inhibit endogenous promoters containing AP-1 response elements but did not affect genes lacking an AP-1 response element

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