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MilliporeSigma

PF0100

Protease Fluorescent Detection Kit

high sensitivity assay

Synonyme(s) :

Protease Assay Kit

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A propos de cet article

NACRES:
NA.26
UNSPSC Code:
12352202
Service technique
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Quality Level

shipped in

dry ice

storage temp.

−20°C

Application

Detection limit: approx. 50 ng trypsin
Protease Fluorescent Detection Kit has been used:
  • in the detection of proteolytic activity using casein based protease assay
  • for testing the extracellular proteolytic activity of fungal strains
  • for quantifying mitochondrial protease activity
  • for measuring the protease production from soil solution

Preparation Note

Supplied with sufficient reagents for up to 200 one mL assays.

The trichloroacetic acid (TCA) component is provided as 6.1 N TCA solution. 0.6 N TCA Solutions may be prepared by a 10-fold dilution of the desired volume of T0699 with ultrapure water. It is not necessary to dilute the entire volume of T0699 for immediate use of the kit.

Analysis Note

Tested for detection of all four proteolytic classes (serine, apartic, cysteine and metalloproteinases).


Composants de kit seuls

Réf. du produit
Description

  • Incubation buffer 25 mL

  • FITC-casein solution 5 mL

  • Assay buffer 200 mL

  • Protease standard (trypsin) 20 μg

  • FITC control 50 mg

  • Trichloroacetic acid (TCA) solution 30 mL

signalword

Danger

target_organs

Respiratory system

Classe de stockage

8A - Combustible corrosive hazardous materials

flash_point_f

Not applicable

flash_point_c

Not applicable

wgk

WGK 3

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1 - Skin Sens. 1 - STOT SE 3



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Protocoles

Protease Fluorescent Detection Kit detects protease activity using FITC-labeled casein substrate.

Articles

Get better detection and quantification of proteases with this high-sensitivity red protease detection assay.


Qiang Fu et al.
Radiation research, 175(6), 728-735 (2011-05-03)
The somatostatin analog SOM230 has potent radioprophylactic and radiation mitigating properties that are unrelated to cytoprotection but appear to be due to suppression of secretion of pancreatic enzymes into the intestinal lumen. To determine the maximal postirradiation time window for
Selena Gimenez-Ibanez et al.
PLoS biology, 12(2), e1001792-e1001792 (2014-02-22)
Pathogenicity of Pseudomonas syringae is dependent on a type III secretion system, which secretes a suite of virulence effector proteins into the host cytoplasm, and the production of a number of toxins such as coronatine (COR), which is a mimic
Martin H Kunzmann et al.
Molecular bioSystems, 8(11), 3061-3067 (2012-09-20)
α-Alkylidene-γ-butyrolactones are quite common in nature and exhibit a broad spectrum of biological activities. We therefore synthesized a small library of xanthatine inspired α-alkylidene-γ-butyrolactones to screen non-pathogenic and uropathogenic E. coli strains by activity based protein profiling (ABPP). The identified



Numéro d'article de commerce international

RéférenceGTIN
PF0100-1KT04061834413271