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Die folgenden MAPmates™ sollten nicht zusammen analysiert werden: -MAPmates™, die einen unterschiedlichen Assaypuffer erfordern. -Phosphospezifische und MAPmate™ Gesamtkombinationen wie Gesamt-GSK3β und Gesamt-GSK3β (Ser 9). -PanTyr und locusspezifische MAPmates™, z.B. Phospho-EGF-Rezeptor und Phospho-STAT1 (Tyr701). -Mehr als 1 Phospho-MAPmate™ für ein einziges Target (Akt, STAT3). -GAPDH und β-Tubulin können nicht mit Kits oder MAPmates™, die panTyr enthalten, analysiert werden.
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A cell detachment solution of proteolytic, collagenolytic & DNAse enzymes. The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue.
More>>A cell detachment solution of proteolytic, collagenolytic & DNAse enzymes. The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue. Less<<
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Accumax Cell Counting Solution in DPBS Sterile-filtered Cell Culture Tested
Overview
A cell detachment solution of proteolytic, collagenolytic and DNAse enzymes. Useful on a variety of cells lines however not all cells or cell types are affected by ACCUMAX™, also passage number and confluency can influence how well the reagent does because the amounts and makeup of the collagen extracellular matrix will vary with age and culture state. Because ACCUMAX™ is a more gentle, less univerally proteolytic cleavage mixture reagent amounts and incubation times need to be optimized for each cell system.
The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue and the routine detachment of cells from standard tissue culture plasticware and adhesion coated plasticware, including SmartPlastic™. ACCUMAX™ does not contain mammalian or bacterial derived products.
Each lot of ACCUMAX™ is tested for Sterility (by USP membrane filtration method), enzymatic activity (tested with synthetic chromagenic tetrapeptides) and cell detachment from tissue culture plastic.
ACCUMAX™ has been used successfully on numerous cell types including: CHO, BHK, 293, COS, Sf9, and catfish primary hepatocyte cells.
A cell detachment solution of proteolytic, collagenolytic & DNAse enzymes. The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue.
Application Notes
A. Cell Counting.
1. Thaw ACCUMAX™ at room temperature.
2. Harvest a representative sample of clumped cells, 0.5 or 1.0 ml, and place in the container used for cell counting.
3. Add an equal volume of ACCUMAX™ to the sample of cells, and incubate for 5 to 10 minutes at 37° C.
4. Count the cells by your normal procedure. Note that the cells have been diluted an extra 2 fold.
5. Count cells and passage as usual; no additional washes or enzyme inhibitors are required.
B. Primary Tissue Dissociation.Recent research has revealed some unique properties of the enzymes contained in ACCUMAX™. The ACCUMAX™ enzymes are more effective at room temperature than at 37°C. In fact, the ACCUMAX™ enzymes will be inactivated after two hours at 37°C. For this reason, perform all your tissue digestion at room temperature.
This protocol for using ACCUMAX™ to dissociate cells from primary tissue is a general-purpose protocol and may not be applicable to all tissue types. The individual investigator needs to optimize the conditions for his/her tissue specimens. Keep in mind that ACCUMAX™ is a powerful enzyme mixture that can potentially dissolve not only the connective tissue of solid tissue but some fragile cell types as well if not closely monitored.
Optimal incubation times and reagent strength needs to be determined for each cell/tissue type tested by the enduser.
Non-sterile materials required:
Platform rocker; Microscope; Centrifuge; Trypan Blue
Culture medium; Scalpels; Pipettes (1 ml, 10 ml); Forceps; Petri dishes (100 mm, non-tissue culture grade)
Procedure:
1. Transfer the tissue to a petri dish containing fresh, sterile DPBS, and rinse.
2. Transfer the tissue to a second dish; dissect off unwanted tissue, such as fat or necrotic material.
3. Using two crossed scalpels or a scalpel and forceps, cut the tissue into small pieces approximately 1 mm in size.
4. Transfer the tissue pieces to a 15 or 50 ml sterile centrifuge tube containing fresh, sterile DPBS.
5. Allow the pieces to settle and carefully remove the supernatant. Repeat this wash step two times.
6. Transfer the tissue pieces to a fresh petri dish and add enough ACCUMAX™ to the plate to cover tissue.
7. Incubate the samples on a platform rocker at room temperature for 5 to 60 minutes. The tissue will “smear” on the bottom of the dish when the disaggregation is effective. To release more cells, gently agitate the sample by pipetting several times. It is best to check cell viability several times during the incubation using Trypan blue.
8. Once disaggregation is complete, transfer the cells to a sterile centrifuge tube and centrifuge at 300 x g to pellet the cells and to remove the cell debris if desired.
9. Carefully remove the supernatant and re-suspend the cell pellet in 5 ml of DMEM/F12 containing 10 – 20% FBS (or other appropriate media). Seed in a T25 flask. Replace the media after 48 hours.
For Soft Tissue samples:
1. If cell isolation is from a soft tissue (such as liver), transfer the tissue to a petri dish containing fresh, sterile DPBS, and rinse.
2. Transfer the tissue to a second dish; dissect off unwanted tissue, such as fat or necrotic material. Add 1 – 2 ml of ACCUMAX ™ and use forceps to gently “tease” the cells into the ACCUMAX™.
3. Residual connective tissue may be separated by allowing the pieces to settle or by filtration, if desired.
4. Centrifuge the sample at 300 x g to pellet the cells and to remove cell debris if desired.
5. Carefully remove the supernatant and re-suspend the cell pellet in 5 ml of DMEM/F12 containing 10 – 20% FBS (or other appropriate media). Seed in a T25 flask. Replace the media after 48 hours.
Biological Information
Media Form
Liquid
Stem Cell Type
Mouse Embryonic Stem Cells
Human Embryonic Stem Cells
Mesenchymal Stem Cells
Neural Stem Cells
Hematopoietic Stem Cells
Epithelial Cells
Pancreatic Stem Cells
Cardiac Stem Cells
Induced Pluripotent Stem Cells
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage Conditions
Stable when stored at -20°C. Refer to lot expiration date. Recommended storage upon receipt is -20°C. After thawing, ACCUMAX may be stored for up to 2 months at 4°C. DO NOT STORE AT ROOM TEMP. Use sterile technique when handling.
What is the difference between Accuma and Accutase?
Accumax (Catalog #SCR006) will dissociate clumped cells in minutes resulting in a single cell suspension. It will yield accurate reproducible cell counts, is cost effective and is ready to use. The Accutase (Catalog #SCR005) contains phenol red. It will detect adherent cells within minutes and will dissociate tissues for primary cell culture use. It also will yield accurate reproducible cell counts, is cost effective and is ready to use.
