Call: +7 771 977 66 65, +7 705 421 2277
Sign in or Register
My basket

Astana Biomed Group, an authorized Abcam distributor in Central Asia

Abiomed homepage

  • Categories
    Signal Transduction
    Cancer
    Epigenetics and Nuclear Signaling
    Immunology
    Cell Biology
    Cardiovascular
    Neuroscience
    Tags & Cell Markers
    Kits/ Lysates/ Other
    Developmental Biology
    Microbiology
    Biochemicals
    Secondary antibodies
    Isotype/Loading Controls
    Antibody Arrays
  • About us
  • Partners
  • Contact
    Address

    Saryarka 32, 18, 010000, Astana city, Kazakhstan

    Telephone +7 771 977 66 65, +7 705 421 2277

    Email

    laboratory@ctlab.kz, orders@abiomed.kz

Back to category

Cellulase Activity Assay kit (Fluorometric) (ab189817)

Price and availability

331 689 ₸

Availability

Order now and get it on Thursday February 25, 2021

Cellulase Activity Assay kit (Fluorometric) (ab189817)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Assay type: Enzyme activity (quantitative)
  • Detection method: Fluorescent
  • Platform: Microplate reader
  • Sample type: Tissue Lysate

You may also be interested in

Product image
Mitochondrial Staining Kit - Orange Fluorescence - Cytopainter (ab112144)
Product image
Anti-ABCG5 antibody [EPR6203] - BSA and Azide free (ab248074)
Product image
Annexin V-mFluor Blue 570 Apoptosis Staining / Detection Reagent (ab219914)
Product image
Recombinant Human GDF15 protein (ab269155)

Overview

  • Product name

    Cellulase Activity Assay kit (Fluorometric)
  • Detection method

    Fluorescent
  • Sample type

    Tissue Lysate
  • Assay type

    Enzyme activity (quantitative)
  • Species reactivity

    Reacts with: Plants
  • Product overview

    Cellulase Activity Assay Kit (Fluorometric) (ab189817) provides a simple method to measure cellulase activity in plant tissues, as well as purified cellulase extracted from plants, bacteria or fungi. The assay uses a long-wavelength fluorescent substrate, resorufin cellobioside. Upon cleavage of the substrate by cellulases present in the sample, the fluorescent compound resorufin is released and fluorescence can be easily detected at Ex/Em = 530/595 nm (peak Ex/Em = 571/585 nm) in a fluorescent microplate reader. The amount of fluorescence will correlate with cellulase activity.

  • Notes

    Cellulases (EC 3.2.1.4) are a family of enzymes that include ß-Glucosidases, endoglucanases, and exoglucanases. These enzymes cleave the ß-1,4-D-glycosidic bonds that link the glucose units comprising cellulose. In addition to being produced by plants, cellulase activity is found in many fungi and bacteria, including some plant pathogens. Most animal cells are not known to produce cellulase; cellulolytic activity is often carried out in animals by symbionts. However, recent evidence does suggest cellulase production in some animals, such as insects and arthopods. The study of cellulase activity has many applications in plant molecular biology, agriculture, and manufacturing. Cellulase is also becoming important in the development of alternative fuel sources, as glucose obtained from cellulose hydrolysis is easily fermented into ethanol.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 200 tests
    DMSO 1 x 5ml
    Reaction Buffer 1 x 30ml
    Reference Standard 1 x 250µl
    Stop Buffer 1 x 10ml
    Substrate Reagent 1 x 1ml

Images

  • Cellulase Assay of Arabidopsis thaliana using Resorufin Cellobioside.
    Cellulase Assay of Arabidopsis thaliana using Resorufin Cellobioside.

    Flowering buds from two mature Arabidopsis thaliana plants (strain CS-20) were removed (0.09 g tissue) and ground to a fine powder in liquid nitrogen. Powder was suspended in Reaction Buffer (200 μL) and centrifuged (13000 rpm) for 10 minutes. Supernatant was
    collected and added in triplicate (50 μL) to wells on a 96-well microtiter plate (clear, flat bottom). A 0.5 mM substrate solution was prepared by diluting Substrate Reagent 1:10 in Reaction Buffer and added to wells (50 μL/well). Fluorescence was recorded with 550nm excitation filter and 595nm emission filter. Fluorescence readings were taken at 3-minute intervals for 120 minutes. Fluorescence values of blank (50 μL Substrate Reagent added to 50 μL Reaction Buffer) were subtracted at each time point.

  • Cellulase Assay using Resorufin Cellobioside.
    Cellulase Assay using Resorufin Cellobioside.

    Several dilutions of purified cellulase from Trichoderma reesei were prepared in Reaction Buffer . Each preparation was added in triplicate (50 μL) to wells on a 96-well microtiter plate (clear, flat bottom). A 0.5 mM substrate solution was prepared by diluting Substrate Reagent 1:10 in Reaction Buffer and added to wells (50 μL/well). Fluorescence was recorded with 550nm excitation filter and 595nm emission filter. Fluorescence readings were taken at 1-minute intervals for 30 minutes. Fluorescence values of blank (50 μL substrate reagent added to 50 μL reaction buffer) were subtracted at each time point.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

Clear all

Recently viewed products

  •  
  • Product image

    Recombinant Human FGE protein (denatured) (ab115708)

Get resources and offers direct to your inbox Sign up
© 2021 Astana Biomed Group LLP. All rights reserved.