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主營產(chǎn)品: Flexcell細胞力學和regenhu細胞3D生物打印機銷售技術服務: 美國Flexcell品牌FX-5000T細胞牽張應力加載培養(yǎng)系統(tǒng),F(xiàn)X-5K細胞顯微牽張應力加載培養(yǎng)系統(tǒng),Tissue Train三維細胞組織培養(yǎng)與測試系統(tǒng),F(xiàn)X-5000C三維細胞組織壓應力加載培養(yǎng)系統(tǒng),STR-4000細胞流體剪切應力加載培養(yǎng)系統(tǒng),德國cellastix品牌Optical Stretcher高通量單細胞牽引應變與分析系統(tǒng) Regenhu品牌3D discovery細胞友好型3D生物打印機,piuma細胞納米壓痕測試分析、aresis多點力學測試光鑷,MagneTherm細胞腫瘤電磁熱療測試分析系統(tǒng)
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LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805)

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  • 產(chǎn)品名稱:LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805)
  • 產(chǎn)品型號:valasciences 4805
  • 產(chǎn)品展商:valasciences
  • 產(chǎn)品文檔:無相關文檔
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LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805) Availability: In Stock — Size: 500 tests using 96 well plates

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LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805)

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Availability: In Stock — Size: 500 tests using 96 well plates

Description

Lipid droplets are the primary fat storage organelles of fat cells (adipocytes). Lipid droplet size, and number are altered by anti-diabetic and anti-obesity drugs and these effects can be quantified utilizing Vala Science Inc's Lipid Droplet Kit. The kit can be utilized to quantify lipid droplets in human primary adipocytes, murine 3T3L1 adipocytes, as well as primary or immortalized hepatocytes.

 

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Contents

Sufficient for five 96-well dishes.

Reagent A: Fixative 60 ml
CAUTION: CONTAINS 4% PARAFORMALDEHYDE - OPEN AND USE IN A WELL-VENTILATED SPACE. AVOID CONTACT AND DISPOSE OF PROPERLY
Reagent B: Permeabilizer 60 ml
Reagent C: Lipid stain 18 ml base solution; 60 μl of 333X stock
Reagent D: Nuclear stain 60 ml

Protocol

  • Fix cells: Remove test solutions, rinse wells with 200 μl/well of cold PBS, add 100 μl of Reagent A per well. Incubate the cells with Reagent A for 15 minutes at room temperature. Rinse wells 1X with 200 μl of PBS to remove fixative.
  • Permeabilize cells: Add 100 μl/well Reagent B. Incubate at 37 C for 15 mins with rotation. Remove Reagent B.
  • Stain the lipid droplets: Vortex Reagent C 333X stock solution thoroughly. Prepare dilution of Reagent C by adding 3 μl of 333X stock solution per ml of base solution, just prior to use. Add 100 μl/well Reagent C. Incubate at 37 C for 60 mins with rotation. Remove Reagent C. Rinse 3X with PBS.
  • Stain nuclei: Add 100 μl/well of Reagent D. Incubate 20 minutes at room temperature. The cells are now ready for imaging.

Imaging

Refer to the manual of your microscopy workstation for image acquisition. Avoid overexposing the images. We typically image adipocytes using a 40X objective. Sharp focus is critical! For each field of view, make sure to image the cells in two fluorescence channels (blue and green). Visualize nuclei on the "blue" channel (excitation filter centered at 360 nm, emitting at 460 nm). Visualize lipid droplets on the "green" channel (excitation at 490 nm, emitting at 520 nm).

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