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Merck
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539132

Millipore

Protease Inhibitor Cocktail II

lyophilized, for the inhibition of aspartic, cysteine, serine, metalloproteases and aminopeptidases. 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 II, The Protease Inhibitor Cocktail Set II controls the activity of Protease. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

Niveau de qualité

Forme

lyophilized

Fabricant/nom de marque

Calbiochem®

Conditions de stockage

OK to freeze
desiccated (hygroscopic)

Conditions d'expédition

wet ice

Température de stockage

−20°C

Description générale

A cocktail of five 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 bacterial cell extracts.
Note: 1 set = 1 vial of lyophilized protease inhibitor cocktail and 1 vial DMSO, 1 ml; 5 sets = 5 vials of lyophilized protease inhibitor cocktail and 5 vials of DMSO, 1 ml.
Protease Inhibitor Cocktail Set II is a specially formulated cocktail of five protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine and metalloproteases as well as aminopeptidases. This cocktail is recommended for use with bacterial cell extracts.

1 set (1 vial of protease inhibitor cocktail plus 1 vial of 1.0 ml DMSO)

5 sets (5 vials of protease inhibitor cocktail plus 5 vials of 1.0 ml DMSO)

Spécificité

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

Application

Protease Inhibitor Cocktail Set II, contains five protease inhibitors for aspartic, cysteine, serine, metalloproteases, and aminopeptidases. Recommended bacterial cell extracts.

Actions biochimiques/physiologiques

Cell permeable: no
Primary Target
Aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases

Avertissement

Toxicity: Irritant (B)

Reconstitution

Following reconstitution, aliquot and freeze at -20°C. The reconstituted material is stable for up to 6 months at -20°C.
This product is provided as a lyophilized solid, ready for reconstitution. For the researcher′s convenience, this protease inhibitor cocktail is provided as either a single vial plus one vial of 1.0 ml DMSO or as a set of 5 vials plus 5 vials of 1.0 ml DMSO. Reconstitute each vial of lyophilized protease inhibitor cocktail with 1 ml of DMSO first. Mix gently. Then add 4 ml of water. The solution will appear turbid.

Informations légales

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

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2

Code de la classe de stockage

10 - Combustible liquids

Point d'éclair (°F)

188.6 °F

Point d'éclair (°C)

87 °C


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Serena Vella et al.
The international journal of biochemistry & cell biology, 76, 1-11 (2016-05-02)
Cardiac progenitors, such as cardiospheres and cardiosphere-derived cells, represent an attractive cell source for cardiac regeneration. The PIWI-interacting RNAs, piRNAs, are an intriguing class of small non-coding RNAs, implicated in the regulation of epigenetic state, maintenance of genomic integrity and
Kevin Molloy et al.
Frontiers in immunology, 11, 198-198 (2020-03-13)
Stenotrophomonas maltophilia is a Gram-negative opportunistic pathogen that can chronically colonize the lungs of people with cystic fibrosis (CF) and is associated with lethal pulmonary hemorrhage in immunocompromised patients. Its secreted virulence factors include the extracellular serine proteases StmPR1, StmPR2
Ilaria Zuliani et al.
International journal of molecular sciences, 22(7) (2021-05-01)
The disturbance of protein O-GlcNAcylation is emerging as a possible link between altered brain metabolism and the progression of neurodegeneration. As observed in brains with Alzheimer's disease (AD), flaws of the cerebral glucose uptake translate into reduced protein O-GlcNAcylation, which

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