P8849
Protease Inhibitor Cocktail
DMSO solution, for the inhibition of serine, cysteine, aspartic, aminopeptidases and thermolysin-like activities, for use in purification of Histidine-tagged proteins, DMSO solution
Synonym(s):
Protease inhibitor solution
เข้าสู่ระบบ เพื่อดูราคาสำหรับองค์กรและสัญญา
เลือกขนาด
เปลี่ยนการดู
เกี่ยวกับสินค้านี้
Form:
DMSO solution
Solubility:
water: soluble
Storage temp.:
−20°C
บริการทางเทคนิค
ต้องการความช่วยเหลือหรือไม่ ทีมนักวิทยาศาสตร์ที่มีประสบการณ์ของเราอยู่ที่นี่เพื่อคุณ
ให้เราช่วยเหลือชื่อสินค้า
Protease Inhibitor Cocktail, for use in purification of Histidine-tagged proteins, DMSO solution
biological source
synthetic
Quality Level
form
DMSO solution
solubility
water: soluble
storage temp.
−20°C
General description
DMSO solution designed for use in the purification of histidine-tagged proteins.
The cocktail contains a mixture of inhibitors that specifically target serine, cysteine, aspartic, and thermolysin-like proteases, and aminopeptidases.
The cocktail contains a mixture of inhibitors that specifically target serine, cysteine, aspartic, and thermolysin-like proteases, and aminopeptidases.
Application
The cocktail has been optimized and tested for isolation of histidine-tagged proteins, with chelating agents omitted for compatibility with IMAC applications.
It is recommended for inhibition of protease activity in 100 mL of cell lysate from 20 g of Escherichia coli or 10 g of baculovirus-infected Spodoptera frugiperda pupal ovary cells.
It is recommended for inhibition of protease activity in 100 mL of cell lysate from 20 g of Escherichia coli or 10 g of baculovirus-infected Spodoptera frugiperda pupal ovary cells.
Biochem/physiol Actions
Inhibits serine, cysteine, aspartic, and thermolysin-like proteases, and aminopeptidases.
Features and Benefits
Specifically formulated for histidine-tagged protein purification.
Targets multiple types of proteases, ensuring comprehensive inhibition of protease activity.
Compatibility with IMAC applications due to omission of chelating agents.
Supplied in convenient packaging options.
Targets multiple types of proteases, ensuring comprehensive inhibition of protease activity.
Compatibility with IMAC applications due to omission of chelating agents.
Supplied in convenient packaging options.
Preparation Note
One mL is recommended for the inhibition of proteases extracted from 20 g of Escherichia coli or 10 g of baculovirus-infected Spodoptera frugiperda pupal ovary cells in a total volume of 100 ml.
This protease inhibitor cocktail has been optimized and tested for histidine-tagged proteins
This protease inhibitor cocktail has been optimized and tested for histidine-tagged proteins
This product is supplied as a clear solution in DMSO. One mL of solution is recommended for inhibition of protease activity in 100 mL of cell lysate from 20 g of E. coli cells or 10 g of baculovirus-infected cells.
Other Notes
AEBSF
Bestatin
E-64
Pepstatin A
Phosphoramidon
Bestatin
E-64
Pepstatin A
Phosphoramidon
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คลาสการจัดเก็บ
10 - Combustible liquids
wgk
WGK 1
flash_point_f
185.0 °F - closed cup
flash_point_c
85 °C - closed cup
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เนื้อหาที่เกี่ยวข้อง
เลือกประเภทตัวยับยั้งโปรตีเอสที่แตกต่างกันตามความต้องการของคุณเพื่อป้องกันการย่อยสลายโปรตีนในระหว่างการแยกและการกำหนดลักษณะและปกป้องโปรตีนในการเตรียมตัวอย่าง
Select different protease inhibitor types based on your needs to prevent protein degradation during isolation and characterization and safeguard proteins in sample prep.
E Boudreau et al.
The EMBO journal, 19(13), 3366-3376 (2000-07-06)
The psbD mRNA, which encodes the D2 reaction center polypeptide of photosystem II, is one of the most abundant chloroplast mRNAs. We have used genomic complementation to isolate the nuclear Nac2 gene, which is required for the stable accumulation of
C Rivier et al.
The EMBO journal, 20(7), 1765-1773 (2001-04-04)
In Chlamydomonas reinhardtii, the psaA mRNA is assembled by a process involving trans-splicing of separate transcripts, encoded at three separate loci of the chloroplast genome. At least 14 nuclear loci and one chloroplast gene, tscA, are needed for this process.
Intracellular Nogo-A facilitates initiation of neurite formation in mouse midbrain neurons in vitro.
Z Kurowska et al.
Neuroscience, 256, 456-466 (2013-10-26)
Nogo-A is a transmembrane protein originally discovered in myelin, produced by postnatal CNS oligodendrocytes. Nogo-A induces growth cone collapse and inhibition of axonal growth in the injured adult CNS. In the intact CNS, Nogo-A functions as a negative regulator of