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Merck

524627

Millipore

Phosphatase Inhibitor Cocktail III

liquid, for the inhibition of serine/threonine and protein tyrosine phosphatases

別名:

Phosphatase Inhibitor Mix (Set III), Phosphatase inhibitor

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About This Item

UNSPSCコード:
12352200
NACRES:
NA.77

product name

Phosphatase Inhibitor Cocktail Set III, Phosphatase Inhibitor Cocktail Set III is a ready to use cocktail of four phosphatase inhibitors for broad-spectrum inhibition of both serine/threonine and protein tyrosine phosphatases.

形状

liquid

メーカー/製品名

Calbiochem®

保管条件

OK to freeze

輸送温度

wet ice

保管温度

−20°C

詳細

Phosphorylation and dephosphorylation regulate signal transduction processes involved in cellular activities such as cell division, proliferation, and apoptosis. Protein kinases add a phosphate group to specific amino acid residues (serine, threonine, or tyrosine) on target proteins, changing their conformation and interaction with ligands. Protein phosphatases remove the phosphate group, restoring the protein to its dephosphorylated state. When extracting phosphorylated proteins from cell and tissue lysates, it is crucial to maintain their phosphorylation status intact. Phosphatase Inhibitor Cocktail Set III is a cocktail of four phosphatase inhibitors for broad-spectrum inhibition of both serine/threonine and protein tyrosine phosphatases. Available as a 1 ml vial or as a set of five 1 ml vials.

アプリケーション

Phosphatase Inhibitor Cocktail Set III has been used:
  • as a supplement in lysis buffer to prepare protein lysates of whole testes for western blotting
  • to fortify ice-cold lysis radio-immunoprecipitation assay (RIPA) buffer to homogenize larval hindguts for western blot analysis
  • as a component in cell lysis buffer to extract total proteins for western blotting

生物化学的/生理学的作用

Cell permeable: no
Primary Target
Serine/threonine and protein tyrosine phosphatases
Product does not compete with ATP.
Reversible: no

特徴および利点

  • Ready-to-use formulations for convenient use
  • High-quality products for consistent and reproducible performance,
  • Flexible options with a range of cocktails targeting different categories of phosphatases

構成

Each vial contains 1 ml of aqueous solution with the following components:
  • 50 mM Sodium Fluoride
  • 10 mM ß-Glycerophosphate (Cat. No. 35675)
  • 10 mM Sodium Pyrophosphate Decahydrate
  • 1 mM Sodium Orthovanadate

警告

Toxicity: Toxic (F)

物理的形状

In H₂O.

再構成

For long-term storage, aliquot and freeze (-20°C). Dilute 1:5 just prior to use.

法的情報

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

保管分類コード

12 - Non Combustible Liquids

WGK

WGK 2

引火点(°F)

Not applicable

引火点(℃)

Not applicable


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

労働安全衛生法名称等を通知すべき危険物及び有害物

名称等を通知すべき危険物及び有害物

Jan Code

524627-1SET:
524627-1SML:
524627-1ML:
524627-1EA:


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

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文書ライブラリにアクセスする

HDAC Inhibition Restores Response to HER2-Targeted Therapy in Breast Cancer via PHLDA1 Induction.
Clayton, et al.
International Journal of Molecular Sciences, 24 (2023)
Lucie Knoblochova et al.
EMBO reports, 24(10), e56530-e56530 (2023-09-11)
After fertilization, remodeling of the oocyte and sperm genomes is essential to convert these highly differentiated and transcriptionally quiescent cells into early cleavage-stage blastomeres that are transcriptionally active and totipotent. This developmental transition is accompanied by cell cycle adaptation, such
HLA-G regulates the invasive properties of JEG-3 choriocarcinoma cells by controlling STAT3 activation
Liu X, et al.
Placenta, 34(11), 1044-1052 (2013)
Blockade of Toll-like receptor 4 (TLR4) reduces oxidative stress and restores phospho-ERK1/2 levels in Leydig cells exposed to high glucose
Karpova T, et al.
Life Sciences, 245, 117365-117365 (2020)
Sarath Ramachandran et al.
Nature communications, 14(1), 6345-6345 (2023-10-11)
The Src homology 2 (SH2) domain recognizes phosphotyrosine (pY) post translational modifications in partner proteins to trigger downstream signaling. Drug discovery efforts targeting the SH2 domains have long been stymied by the poor drug-like properties of phosphate and its mimetics.

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