Loading...
Products:Signal Transduction >> Metabolism >> Mitochondrial
MSCatalog No. MSX31-30
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »MetaPath™ Mito Disease 4-Plex Dipstick Array
Cell culture extracts, Tissue
Quantitative
0h 30m
Reacts with
Human
ab109879 (MSX31) is a novel array that allows for the simultaneous quantification of 4 key enzymes whose expression is down-regulated in different mitochondrial diseases: Complex I, Complex IV, PDH and Frataxin. The array is comprised of 4 monoclonal capture antibodies striped onto a dipstick, and the immunocaptured sample is detected using 4 monoclonal detector antibodies that recognize different epitopes on the target enzymes. This array is very rapid (total assay time including sample prep is less than 1 hour) and very sensitive, and as with all Abcam's assays, isolation of mitochondria is not required.
This array is suitable for testing a variety of sample types. Not only is it useful for measuring samples that are deficient in the 4 enzymes due to genetic mutations, it is also useful for measuring changes in the expression of the enzymes due to drug treatments or other manipulations.
Sandwich ELISAmore details
Please see Notes section
| Components | 90 tests | 30 tests |
|---|---|---|
| Buffer A (Extraction buffer) | 1 x 45ml | 1 x 15ml |
| Buffer B (10X Blocking solution) | 1 x 1.2ml | 1 x 0.4ml |
| Buffer C (Wash buffer) | 6 x 1ml | 2 x 1ml |
| Dipsticks | 1 x 90 units | 1 x 30 units |
| Gold-conjugated antibody (dried in microplate wells) | 1 x 90 tests | 1 x 30 tests |
Our Abpromise guarantee covers the use of ab109879 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
sELISA
ELISA - MetaPath™ Mito Disease 4-Plex Dipstick Array (ab109879)

A typical standard curve for ab109879 using HepG2 cell extract. We suggest using 7 to 8 dipsticks for covering the working range. In this example, the maximum sample load should be 5 µg linear regression above which non-linear regression should be used.
ELISA - MetaPath™ Mito Disease 4-Plex Dipstick Array (ab109879)

Examples of dipsticks from (a) normal fibroblast cells (b) rho0 fibroblast cells which lack mtDNA and hence complexes I and IV only (c) a fibroblast sample from a patient exhibiting a specific deficiency in complex I (d) pure frataxin and (e) buffer control with containing no sample. Data from these sticks was collected using a simple flatbed scanner and ImageJ software.
Sandwich ELISA - MetaPath™ Mito Disease 4-Plex Dipstick Array (ab109879)

Dipstick assays use the well-established lateral flow concept, whereby capture antibodies are striped onto nitrocellulose membrane and a Whatman paper wicking pad draws the sample through the antibody bands. Detector antibodies, conjugated to gold, are dried in the wells of a 96-well plate. Sample is added to the well, the dipstick inserted, and within minutes the line for each target is revealed as the protein-detector antibody-gold complex binds with the capture antibodies. Multiplexing dipstick assays have multiple target protein lines. A positive control goat anti-mouse antibody line is included on all assays to ensure that adequate wicking of the sample occurred.
This product has been referenced in:
See 1 publication for this product
Publishing research using ab109879? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:

A typical standard curve for ab109879 using HepG2 cell extract. We suggest using 7 to 8 dipsticks for covering the working range. In this example, the maximum sample load should be 5 µg linear regression above which non-linear regression should be used.

Examples of dipsticks from (a) normal fibroblast cells (b) rho0 fibroblast cells which lack mtDNA and hence complexes I and IV only (c) a fibroblast sample from a patient exhibiting a specific deficiency in complex I (d) pure frataxin and (e) buffer control with containing no sample. Data from these sticks was collected using a simple flatbed scanner and ImageJ software.

Dipstick assays use the well-established lateral flow concept, whereby capture antibodies are striped onto nitrocellulose membrane and a Whatman paper wicking pad draws the sample through the antibody bands. Detector antibodies, conjugated to gold, are dried in the wells of a 96-well plate. Sample is added to the well, the dipstick inserted, and within minutes the line for each target is revealed as the protein-detector antibody-gold complex binds with the capture antibodies. Multiplexing dipstick assays have multiple target protein lines. A positive control goat anti-mouse antibody line is included on all assays to ensure that adequate wicking of the sample occurred.
0
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
