Bio-rad Bio-Plex Pro™ Rat Cytokine, Chemokine, and Growth Manuel d'utilisateur

Naviguer en ligne ou télécharger Manuel d'utilisateur pour Accessoires pour l'eau Bio-rad Bio-Plex Pro™ Rat Cytokine, Chemokine, and Growth . Bio-Rad Bio-Plex Pro™ Rat Cytokine, Chemokine, and Growth Factor Assays User Manual Manuel d'utilisatio

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This guide can be used to prepare and run a full 1 x 96-well assay plate.
Refer to the complete instruction manual for more information on a given
step. New users can download the manual, which includes detailed
instructions and a list of kit components, at www.bio-rad.com/bio-plex.
Initial Preparation
1. Plan the plate layout.
2. Start up/warm up the Bio-Plex
®
system (30 min).
n
Bring assay buffer, wash buffer, and sample diluent to room
temperature (RT). Keep other items on ice until needed
n
Begin to thaw frozen samples
3. Prime wash station for flat bottom plate or set vacuum manifold to
–1 to –3" Hg for filter plate.
4. Calibrate the Bio-Plex system by following the prompts within
Bio-Plex Manager
software. This can be done now or during an
assay incubation step.
5. Reconstitute a single vial of standards in 500 µl of a diluent similar to the
final sample type or matrix. Vortex for 5 sec and incubate on ice for 30 min.
Bio-Plex Pro
Assays
Quick Guide 4
IMPORTANT! Pay close attention to vortexing, shaking, and incubation instructions.
Deviation from the protocol may result in low assay signal and assay variability.
For use with Instruction Manual #
Human, Mouse, and Rat Cytokine Assays 10014905
Sample Type Diluent for Standards Add BSA
Serum and plasma Standard diluent None
Culture media, with serum Culture media None
Culture media, serum-free Culture media To 0.5% final (w/v)
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Résumé du contenu

Page 1 - Bio-Plex Pro

This guide can be used to prepare and run a full 1 x 96-well assay plate. Refer to the complete instruction manual for more information on a given

Page 2

6. Prepare a fourfold standard dilution series and blank as shown below. Vortex for 5 sec between liquid transfers. If mixing diabetes assays with

Page 3 - Running the Assay

Running the Assay 1. Prewet filter plate with 100 µl Bio-Plex assay buffer (skip for flat bottom). 2. Vortex the diluted (1x) beads for 10–20 sec.

Page 4 - Laboratories, Inc

11. Wash the plate three times with 100 µl wash buffer. 12. Vortex the diluted (1x) SA-PE. Add 50 µl to each well.13. Repeat Step 5. See table for in

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