524632
Phosphatase Inhibitor Cocktail V
50X, lyophilized solid, for the inhibition of acid, alkaline, serine/threonine and protein tyrosine phosphatases. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
同義詞:
Phosphatase inhibitor cocktail
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About This Item
推薦產品
product name
Phosphatase Inhibitor Cocktail Set V, 50X, Lyophilized, The Phosphatase Inhibitor Cocktail Set V, 50X, Lyophilized controls the activity of Phosphatase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
形狀
lyophilized solid
製造商/商標名
Calbiochem®
儲存條件
OK to freeze
desiccated (hygroscopic)
protect from light
運輸包裝
ambient
儲存溫度
2-8°C
一般說明
A cocktail of four phosphatase inhibitors for broad-spectrum inhibition of acid, alkaline, serine/threonine and protein tyrosine phosphatases. Available as a 1 ml vial or a set of five 1 ml vials. Each vial, when reconstituted with 1 ml H2O contains 250 mM Sodium Fluoride, 50 mM β-Glycerophosphate (Cat. No. 35675), 50 mM Sodium Pyrophosphate Decahydrate, 50 mM Sodium Orthovanadate.
A cocktail of four phosphatase inhibitors for broad-spectrum inhibition of acid, alkaline, serine/threonine and protein tyrosine phosphatases. Available as a 1 ml vial or a set of five 1 ml vials. Once reconstituted, each vial contains the following components:
包裝
Packaged under inert gas
警告
Toxicity: Toxic (F)
重構
Following reconstitution, aliquot and freeze (-20°C) for long-term storage. Dilute 1:50 just prior to use.
Reconstitute each vial with 1 ml H₂O.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
安全危害
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
International journal of molecular sciences, 23(13) (2022-07-10)
An oversupply of nutrients with a loss of metabolic flexibility and subsequent cardiac dysfunction are hallmarks of diabetic cardiomyopathy. Even if excess substrate is offered, the heart suffers energy depletion as metabolic fluxes are diminished. To study the effects of
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