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QIA108 Caspase-7 Immunoassay/Activity Kit, Fluorometric

QIA108
  
Purchase on Sigma-Aldrich

Overview

Replacement Information

Key Spec Table

Detection Methods
Fluorometric
Description
Overview

This product has been discontinued.





Specifically detects caspase-7 activity using the DEVD-AFC substrate. Caspase-7 substrates such as DEVD will also detect the activity of other caspases including caspase-3. This kit ensures specificity by first capturing caspase-7 using a selective antibody.
Catalogue NumberQIA108
Brand Family Calbiochem®
Materials Required but Not Delivered PBS
References
Product Information
Detection methodFluorometric
Form96 Tests
Format96-well plate
Kit containsCell Lsis Buffer, Coating Buffer, Anti-Caspase-7 Antibody, Blocking Buffer, Incubation Buffer, DTT, DEVD-AFC Substrate, Recombinant Caspase-7, 96-Well Plate, Plate Sealer, and a user protocol.
Applications
Biological Information
Assay time6 h
Sample TypeCultured cells
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
R PhraseR: 22-38-41-52/53

Harmful if swallowed.
Irritating to skin.
Risk of serious damage to eyes.
Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
S PhraseS: 24-26-39-61

Avoid contact with skin.
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear eye/face protection.
Avoid release to the environment. Refer to special instructions/safety data sheet.
Product Usage Statements
Intended useThe Calbiochem® Caspase-7 Immunoassay/Activity Kit is intended for the specific, semi-quantitative detection of caspase-7 activity.
Storage and Shipping Information
Ship Code Dry Ice Only
Toxicity Multiple Toxicity Values, refer to MSDS
Storage -20°C
Storage ConditionsUpon arrival, store the unopened kit at -20°C. Following initial thaw, store the Cell Lysis Buffer, Coating Buffer, Blocking Buffer, and Incubation Buffer at 4°C. Once opened, all components are stable for up to 6 months.
Protect from Light Protect from light
Avoid freeze/thaw Avoid freeze/thaw
Do not freeze Ok to freeze
Packaging Information
Transport Information
Supplemental Information
Kit containsCell Lsis Buffer, Coating Buffer, Anti-Caspase-7 Antibody, Blocking Buffer, Incubation Buffer, DTT, DEVD-AFC Substrate, Recombinant Caspase-7, 96-Well Plate, Plate Sealer, and a user protocol.
Specifications
Global Trade Item Number
Catalogue Number GTIN
QIA108 0

Documentation

Caspase-7 Immunoassay/Activity Kit, Fluorometric Certificates of Analysis

TitleLot Number
QIA108

Brochure

Title
Caspases and other Apoptosis Related Tools Brochure
Kit SourceBook - 2nd Edition EURO
User Protocol

Revision19-September-2008 RFH
Form96 Tests
Format96-well plate
Detection methodFluorometric
Specieshuman, mouse, rat
StorageUpon arrival, store the unopened kit at -20°C. Following initial thaw, store the Cell Lysis Buffer, Coating Buffer, Blocking Buffer, and Incubation Buffer at 4°C. Once opened, all components are stable for up to 6 months.
Intended useThe Calbiochem® Caspase-7 Immunoassay/Activity Kit is intended for the specific, semi-quantitative detection of caspase-7 activity.
Principles of the assayThe Calbiochem® Caspase-7 Immunoassay/Activity Kit utilizes a caspase-7 polyclonal antibody to capture activated caspase-7 from cell lysates. A fluorogenic substrate, DEVD-AFC, is then added to the wells and is cleaved by the captured, active caspase-7. The cleavage generates free AFC that is then analyzed using a fluorescence plate reader with an excitation wavelength of 370-425 nm and an emission wavelength of 490-525 nm. The increase in fluorescence is directly proportional to the caspase-7 activity.

Caspase-7 substrates such as DEVD will also be cleaved by other caspases, including caspase-3. However, by incorporating a specific capture step the assay only measures caspase-7 activity and other known caspases and non-specific proteases are not detected.
Materials provided•Cell Lysis Buffer (Kit Component No. JA7541-25ML): 1 bottle, 25 ml
•Coating Buffer (Kit Component No. JA7542-10ML): 1 bottle, 10 ml
•Anti-Caspase-7 Antibody, 20X (Kit Component No. JA7543-500UL): 1 vial, 500 µl
•Blocking Buffer (Kit Component No. JA7544-15ML): 1 bottle, 15 ml
•Incubation Buffer (Kit Component No. JA7545-100ML): 1 bottle, 100 ml
• DTT (Kit Component No. JA7546-400UL): 1 vial, 400 µl
•DEVD-AFC Substrate (Kit Component No. JA7547-500UL): 1 vial, 500 µl
•Recombinant Caspase-7 (Kit Component No. JA7548-10U): 1 vial, 10 U
•96-Well Plate (Kit Component No. JA7549-EA): 1 plate, 96 wells
•Adhesive Plate Cover (Kit Component No. JA7550-EA): 2 each
Materials Required but not provided PBS
PreparationPreparation of Cell Lysates 1. Induce apoptosis as desired. Include a negative control using uninduced cells. Collect 5x106 cells per assay. 2. Wash cells with ice-cold PBS. Centrifuge at 700 x g. 3. Resuspend cells in 200 µl cold Cell Lysis Buffer. Incubate for 10 min on ice. 4. Centrifuge at 10,000 x g for 1 min. 5. Transfer the supernatant to a clean tube. Use immediately or aliquot and freeze (-20°C). The supernatant can be stored at -20°C for up to 6 months.
Reagent preparation•1X Anti-Caspase-7 Antibody: Prepare the desired amount of 1X Anti-Caspase-7 Antibody by making a 1:20 dilution of the Anti-Caspase-7 Antibody, 20X in Coating Buffer. •Recombinant Caspase-7: Reconstitute the Recombinant Caspase-7 in 10 µl PBS. Dilute 1:100 in Cell Lysis Buffer as needed for the assay.
Detailed protocol1. Add 100 µl 1X Anti-Caspase-7 Antibody to each well. Cover the plate tightly with an Adhesive Plate Cover and incubate at 37°C for 1 h or at 4°C overnight.
2. Remove the antibody solution from the wells.
3. Add 150 µl Blocking Buffer to each well. Cover the plate tightly with an Adhesive Plate Cover and incubate at room temperature for 30 min.
4. Remove the Blocking Buffer and wash the wells 3 times with 150 µl Incubation Buffer.
5. Add 100 µl cell lysate or 1 unit Recombinant Caspase-7 (positive control) to Anti-Caspase-7 Antibody-coated wells. Cover the plate tightly with an Adhesive Plate Cover and incubate at 37°C for 1 h.
6. Remove the solutions from the wells and wash 3 times with 150 µl Incubation Buffer.
7. Add 94 µl Incubation Buffer, 5 µl DEVD-AFC, and 1 µl DTT to each well. Cover the plate tightly with an Adhesive Plate Cover and incubate for 2-4 h at 37°C. Overnight incubation at 37°C may increase sensitivity.
8. Read the samples using a fluorescence plate reader set at an excitation wavelength of 370-425 nm and an emission wavelength of 490-525 nm. Determine the Caspase-7 activity by comparing results with the activity level of the uninduced control.
Registered TrademarksCalbiochem® is a registered trademark of EMD Biosciences, Inc.
Interactive Pathways™ is a trademark of EMD Biosciences, Inc.