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Millipore

Phosphatase Inhibitor Cocktail III

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

Synonim(y):

Phosphatase Inhibitor Mix (Set III), Phosphatase inhibitor

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About This Item

Kod UNSPSC:
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.

Postać

liquid

producent / nazwa handlowa

Calbiochem®

warunki przechowywania

OK to freeze

Warunki transportu

wet ice

temp. przechowywania

−20°C

Opis ogólny

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.

Zastosowanie

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

Działania biochem./fizjol.

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

Cechy i korzyści

  • 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

Komponenty

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

Ostrzeżenie

Toxicity: Toxic (F)

Postać fizyczna

In H₂O.

Rekonstytucja

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

Informacje prawne

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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)
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)
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.
A targeted genetic modifier screen in Drosophila uncovers vulnerabilities in a genetically complex model of colon cancer
Datta I, et al.
G3: Genes, Genomes, Genetics, 13(5), jkad053-jkad053 (2023)
HDAC Inhibition Restores Response to HER2-Targeted Therapy in Breast Cancer via PHLDA1 Induction.
Clayton, et al.
International Journal of Molecular Sciences, 24 (2023)

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