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Sigma-Aldrich

Clostripain from Clostridium histolyticum

≥20 units/mg solid

Synonym(s):

Clostridiopeptidase B, Proteinase from Clostridium histolyticum

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About This Item

CAS Number:
EC Number:
EC Number:
MDL number:
UNSPSC Code:
12352204
NACRES:
NA.54
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form

lyophilized powder

Quality Level

specific activity

≥20 units/mg solid

mol wt

15.4 kDa
41.7 kDa

impurities

salt, essentially free

storage temp.

2-8°C

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639086629412540
Mesitylene analytical standard

63908

Mesitylene

Benzene analytical standard

12540

Benzene

application(s)

environmental

application(s)

environmental

application(s)

environmental

application(s)

environmental

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

format

neat

format

neat

format

neat

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

Application

Clostripain from Clostridium histolyticum has been used as a proteolytic enzyme in perfusate to detect its effect on tube hematocrit.[1] It has also been used in limited proteolysis of DNA polymerase (gp43) of phage T4 (RB69 gp43).[2]

Biochem/physiol Actions

Clostripain from Clostridium histolyticum is composed of two polypeptide chains, with molecular masses of 41.7 kDa and 15.4 kDa. Clostripain has a highly restricted substrate specificity for Arg-Xaa peptide bonds. Therefore, clostripain has been explored as a potential enzyme for protein sequencing purposes. It has also been studied as a catalyst for condensation of pharmaceutically important peptides containing Arg-Pro bonds.[3]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality

Purified, essentially salt-free

Unit Definition

One unit will hydrolyze 1.0 μmole of BAEE per min at pH 7.6 at 25 °C in the presence of 2.5 mM DTT.

Analysis Note

The enzyme must be activated for 2-3 hours before use by dissolving in 2.5 mM dithiothreitol containing 1.0 mM calcium acetate.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Z Korsak et al.
International journal of occupational medicine and environmental health, 9(4), 341-349 (1996-01-01)
Neurotoxic effects of trimethylbenzene isomers (pseudocumene, mesitylene and hemimellitene) in male rats were investigated in conditions of acute and subchronic inhalation exposure. Rotarod performance and pain sensitivity behaviour were tested in rats exposed to trimethylbenzenes at concentrations of 250-2,000 ppm
Z Korsak et al.
International journal of occupational medicine and environmental health, 10(3), 303-311 (1997-01-01)
Sensory respiratory irritation effects of trimethylbenzene isomers (TMBs) (hemimellitene, mesitylene and pseudocumene) in male Balb/C mice were investigated in conditions of acute exposure and in male Wistar rats in conditions of repeated 90-day inhalation exposure to pseudocumene. The pseudocumene, mesitylene
Z Korsak et al.
International journal of occupational medicine and environmental health, 13(3), 223-232 (2000-12-08)
Toxic effects of exposure to 1,2,3-trimethylbenzene (hemimellitene) in the condition of subchronic inhalation experiment were examined. Rats were exposed to vapours of hemimellitene at concentrations of 123 mg/m3, 492 mg/m3 and 1230 mg/m3, 6 h/day, 5 days/week for 3 months.
Y Tsujimoto et al.
Chemosphere, 39(5), 725-730 (1999-08-17)
The structure was investigated of the mercapturic acid excreted in urine of rats after the i.p. administration of 1,2,3-trimethylbenzene. Of the two regioisomeric mercapturic acids, i.e. N-acetyl-S-(2,3-dimethylbenzyl)-L-cysteine and N-acetyl-S-(2,6-dimethyl-benzyl)-L-cysteine, only the former was isolated by preparative HPLC and identified, by
Application of gas chromatography in conjunction with enrichment of samples on active carbon to determine low concentrations of organic compounds in air. Part I. Aromatic hydrocarbons.
H Swedrowska et al.
Bulletin of the Institute of Maritime and Tropical Medicine in Gdynia, 37(1-2), 103-112 (1986-01-01)

Protocols

Protocol for GC Analysis of Hydrocarbons in Gasoline on Petrocol® DH

-Xylene; Nonane; Propylbenzene; Mesitylene; 1,2,4-Trimethylbenzene; 1,2,3-Trimethylbenzene; 1,3-Diethylbenzene; 1,4-Dimethyl-2-ethylbenzene; 1,2-Dimethyl-4-ethylbenzene; Durene; 1,2,3,5-Tetramethylbenzene; 1,2,3,5-Tetramethylbenzene; 2-Methylnaphthalene (β)

GC Analysis of Hydrocarbons in Gasoline on Petrocol® DH, Isothermal

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