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539133

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Protease Inhibitor Cocktail VI

liquid, for the inhibition of proteases and esterases. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

Synonyme(s) :

Protease inhibitor cocktail

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About This Item

Code UNSPSC :
12352200
Nomenclature NACRES :
NA.54

product name

Protease Inhibitor Cocktail Set VI, The Protease Inhibitor Cocktail Set VI controls the activity of Protease. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

Forme

liquid

Fabricant/nom de marque

Calbiochem®

Conditions de stockage

OK to freeze

Conditions d'expédition

wet ice

Température de stockage

−20°C

Description générale

A cocktail of six protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases. This cocktail is recommended for use with plant cell extracts. Each vial contains 200 mM AEBSF, HCl (Cat. No. 101500), 10 mM Bestatin (Cat. No. 200484), 3 mM E-64 (Cat. No. 324890), 2 mM Leupeptin Hemisulfate (Cat. No. 108975), 2 mM Pepstatin A (Cat. No. 516481), and 500 mM 1,10-Phenanthroline (Cat. No. 516705). One ml is recommended for 30 g of various plant tissues. Supplied with a data sheet. Note: 1 set = 5 x 1 ml.
A cocktail of six protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases. This cocktail is recommended for use with plant cell extracts. One ml is recommended for 30 g of various plant tissues.



This cocktail is provided as a single vial of 1 ml, or as a package of 5 x 1 ml vials. Each vial contains the inhibitors solubilized in DMSO at the following concentrations:
The Protease Inhibitor Cocktail Set VI controls the activity of Protease. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

Spécificité

Inhibits a broad spectrum of serine proteases, cysteine proteases, aspartic proteases, and metalloproteases, as well as aminopeptidases.

Actions biochimiques/physiologiques

Primary Target
Aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases.
Product does not compete with ATP.

Avertissement

Toxicity: Toxic (F)

Forme physique

In 1 ml DMSO.

Informations légales

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

Pictogrammes

CorrosionExclamation markEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

188.6 °F

Point d'éclair (°C)

87 °C


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Huimeng Tang et al.
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Mousa Vatanmakanian et al.
Frontiers in endocrinology, 14, 1156120-1156120 (2023-10-30)
Prostate cancer (PCa) presents a significant health challenge in men, with a substantial number of deaths attributed to metastatic castration resistant PCa (mCRPC). Moreover, African American men experience disproportionately high mortality rates due to PCa. This study delves into the
Mingyue Li et al.
Cell death discovery, 9(1), 127-127 (2023-04-15)
Sestrins are a small gene family of pleiotropic factors whose actions promote cell adaptation to a range of stress conditions. In this report we disclose the selective role of Sestrin2 (SESN2) in dampening aerobic glycolysis to adapt to limiting glucose
Salim Abdisalaam et al.
Nucleic acids research, 50(5), 2681-2699 (2022-02-22)
Cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS) is activated in cells with defective DNA damage repair and signaling (DDR) factors, but a direct role for DDR factors in regulating cGAS activation in response to micronuclear DNA is still poorly understood. Here

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