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- 详细信息
- 文献和实验
- 技术资料
- 应用范围:
Activity Assay
- 宿主:
0
- 适应物种:
Human
- 库存:
大量
- 抗原来源:
0
- 是否单克隆:
0
- 规格:
1 plate
NOTE: Optimal assay timing and performance may vary for different cell lines but generally can be obtained using subconfluent cell cultures in the assay described below. Subconfluent cultures can be achieved by splitting cells 1 to 2 days prior to performing the assay.
1. Rehydrate the strips with 200 mL of PBS per well for at least 15 minutes at room temperature. Remove the PBS from the rehydrated strips.
2. Prepare a single cell suspension, preferably using a non-enzymatic dissociation buffer. Optimum cell density may be determined by titration of the cells. A common starting range is between 1x10E05 to 1x10E07 cells/mL.
3. Add 100 mL of the diluted cell suspension to each well. Incubate the plate at 37°C for 1 hour in a CO2 incubator. Gently wash the plate 2-3 times with PBS containing Ca2+/Mg2+ (200 mL/well).
4. Add 100 mL of 0.2% crystal violet in 10% ethanol to each well. Incubate for 5 minutes at room temperature. Remove the stain from the wells. Gently wash the plate 3 times with PBS (300 mL/well).
5. Add 100 mL of Solubilization Buffer (A 50/50 mixture of 0.1M NaH2PO4, pH 4.5 and 50% ethanol) to each well. Allow strips to incubate and gently shake at room temperature until the cell-bound stain is completely solubilized; approximately 5 minutes.
6. Determine the absorbance at 540 - 570 nm on a microplate reader.
- Human Embryonic Stem Cells
- Mouse Embryonic Stem Cells
- Mesenchymal Stem Cells
- Neural Stem Cells
- Hematopoietic Stem Cells
- Epithelial Cells
- Pancreatic Stem Cells
- Induced Pluripotent Stem Cells
- FN1
- DKFZp686O13149
- DKFZp686H0342
- DKFZp686I1370
- MSF
- FN
- CIG
- DKFZp686F10164
- LETS
- FINC
under the CytoMatrixTM brand name.
Product Family Information
ECM Proteins and coated platesMillipore offers a wide variety of ECM proteins and coated cultureware to meet the individual needs of your cell line. Our ECM Cell Culture Optimization Array can help you determine the best coating and concentration for your particular cell type. |
更多产品技术资讯,请访问密理博中国博客:http://blog.milliporechina.com
详细描述见链接:http://www.millipore.com/catalogue/item/ECM101
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文献和实验Dynamic Flow Assay in a Parallel Plate Flow Chamber
Objective lens (6.3 x, 10 x, 40 x) Stage incubator Biological: Cell suspension (neutrophils, cancer cells) Cell monolayer or coated substrate in 35 mm dishes Adhesion media (culture
of 7 x 2 x 0.5" and bottom dimensions of 7 x 2 x 0.25". 2) Recess the top plate in the center portion to 0.125" deep, leaving 0.950" per end for 1.375" wide x 0.3125" deep fluid reservoir. 3) Drill 1/16" wide x 0.625" long
Dynamic Flow Assay in a Parallel Plate Flow&n
(neutrophils, cancer cells) Cell monolayer or coated substrate in 35 mm dishes Adhesion media (culture media serum-free with 12 mM Hepes) Fibronectin (human plasma) Bovine serum albumin (BSA
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