台盼蓝溶液

台盼蓝溶液

    价格:190

    货号:03-102-1B

    规格:100ml

    产品名称:台盼蓝溶液     

      Trypan Blue Solution, 5mg/ml in Saline


   




【产品介绍】

Trypan Blue is the stain most commonly used to distinguish viable from nonviable cells. 

Viable cells exclude the dye, while nonviable cells absorb the dye and appear blue. Cells 

should be in suspension as single cells in buffered saline before counting. Trypan Blue has 

a higher affinity for serum protein than for cellular proteins, so suspending cells in medium 

containing serum will generate a dark background.

使用说明

(用血细胞仪法计数细胞)

1.Aseptically withdraw a sample of the cell suspension and prepare 1:2, 1:5, 1:10, or 1:100 

dilutions as required in Phosphate Buffered Saline (PBS). Dilute 1:5 in 0.5% Trypan Blue. 

The optimal concentration of cells for counting is 5-10X105 cells/ml (50-100 cells per large

 square of the hemocytometer counting chamber) after dilution in the Trypan Blue Solution.

2.After staining with Trypan Blue, the cells should be counted within three (3) minutes; after 

that interim, the non-viable cells will begin to take up the dye.

3.Using a Pasteur pipette, withdraw a small amount of the stained cell suspension and place

 the tip of the pipette onto the slot of a clean hemocytometer with a planar coverslip, thereby 

creating a three-dimensional space. The cell suspension will be transferred under the coverslip

 by capillary action as the fluid is allowed to flow from the capillary under the coverslip to cover

 the area of the grid. Next fill the opposite chamber with the second diluted sample. Do not 

overfill the chamber and do not disturb the coverslip after the hemocytometer has been 'charged.'

4.Place the hemocytometer on the stage of an inverted microscope using the 10X objective. Adjust 

focus until a single counting square fills the field. The etched grid marking the boundaries for the 

counting procedure delineates a specific volume within the space.


说明书下载:

台盼蓝溶液6380680080676747806228420.pdf


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