539138
Protease Inhibitor Cocktail VII
liquid, for the inhibition of serine proteases, cysteine proteases, aspartic proteases and thermolysin-like proteases and aminopeptidases. Recommended for purification of proteins containing His•Tag sequences.
Synonym(s):
Protease inhibitor
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
UNSPSC Code:
12352200
NACRES:
NA.54
Recommended Products
product name
Protease Inhibitor Cocktail Set VII, Protease Inhibitor Cocktail Set VII contains five protease inhibitors with broad specificity. Recommended for purification of proteins containing His•Tag sequences.
form
liquid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
shipped in
wet ice
storage temp.
−20°C
Related Categories
General description
A cocktail of five protease inhibitors with broad specificity for the inhibition of cysteine, serine, aspartic, and thermolysin-like proteases and aminopeptidases. This cocktail is recommended for purification of proteins containing His•Tag sequences. Each vial contains 100 mM AEBSF, HCl (Cat. No. 101500), 5 mM Bestatin (Cat. No. 200484), 1.5 mM E-64 (Cat. No. 324890), 2 mM Pepstatin A (Cat. No. 516481), and 200 µM of Phosphoramidon, Disodium Salt (Cat. No. 525276). One ml is recommended for the inhibition of proteases in 10 g of cells. Supplied with a data sheet. Note: 1 set = 5 x 1 ml.
This set is a specially formulated protease inhibitor cocktail of five protease inhibitors with broad specificity for the inhibition of cysteine, serine, aspartic, and thermolysin-like proteases and aminopeptidases. This cocktail is recommended for purification of histidine-tagged proteins.
This product is provided as a single vial or as a set of 5 vials. Each vial contains 1 ml of protease inhibitor cocktail solubilized in DMSO with the following components:
This product is provided as a single vial or as a set of 5 vials. Each vial contains 1 ml of protease inhibitor cocktail solubilized in DMSO with the following components:
Specificity
Inhibits serine proteases, cysteine proteases, aspartic proteases and thermolysin-like proteases and aminopeptidases.
Warning
Toxicity: Irritant (B)
Physical form
In 1 ml DMSO.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
188.6 °F
Flash Point(C)
87 °C
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Lindsey J Anstine et al.
Cancer research, 83(7), 997-1015 (2023-01-26)
Breast cancer subtypes and their phenotypes parallel different stages of the mammary epithelial cell developmental hierarchy. Discovering mechanisms that control lineage identity could provide novel avenues for mitigating disease progression. Here we report that the transcriptional corepressor TLE3 is a
Tong Wang et al.
Methods in molecular biology (Clifton, N.J.), 2473, 101-128 (2022-07-13)
The entanglement of long axons found in cultured dissociated hippocampal neurons restricts the analysis of the machinery underlying directed axonal trafficking. Further, hippocampal neurons exhibit "en passant" presynapses that may confound the analysis of long-range retrograde axonal transport. To solve
Katrina M Piemonte et al.
The Journal of biological chemistry, 299(7), 104834-104834 (2023-05-19)
Chromatin organization is highly dynamic and modulates DNA replication, transcription, and chromosome segregation. Condensin is essential for chromosome assembly during mitosis and meiosis, as well as maintenance of chromosome structure during interphase. While it is well established that sustained condensin
Christopher R M Asquith et al.
Molecules (Basel, Switzerland), 23(5) (2018-05-23)
We demonstrate for the first time that 4H-1,2,6-thiadiazin-4-one (TDZ) can function as a chemotype for the design of ATP-competitive kinase inhibitors. Using insights from a co-crystal structure of a 3,5-bis(arylamino)-4H-1,2,6-thiadiazin-4-one bound to calcium/calmodulin-dependent protein kinase kinase 2 (CaMKK2), several analogues
Yan Wang et al.
Cell reports. Medicine, 5(6), 101580-101580 (2024-05-23)
Natural killer (NK) cell-based immunotherapy holds promise for cancer treatment; however, its efficacy remains limited, necessitating the development of alternative strategies. Here, we report that venetoclax, an FDA-approved BCL-2 inhibitor, directly activates NK cells, enhancing their cytotoxicity against acute myeloid
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service