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主营产品: Flexcell细胞力学和regenhu细胞3D生物打印机销售技术服务: 美国Flexcell品牌FX-5000T细胞牵张应力加载培养系统,FX-5K细胞显微牵张应力加载培养系统,Tissue Train三维细胞组织培养与测试系统,FX-5000C三维细胞组织压应力加载培养系统,STR-4000细胞流体剪切应力加载培养系统,德国cellastix品牌Optical Stretcher高通量单细胞牵引应变与分析系统 Regenhu品牌3D discovery细胞友好型3D生物打印机,piuma细胞纳米压痕测试分析、aresis多点力学测试光镊,MagneTherm细胞肿瘤电磁热疗测试分析系统
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LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805)

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  • 产品名称:LIPID DROPLET SCREEN-CERTIFIED KIT (CAT. 4805)
  • 产品型号:valasciences 4805
  • 产品展商:valasciences
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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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