LDH细胞毒性检测试剂盒

产品：LDH细胞毒性检测试剂盒
货号：8078

Introduction

Lactate dehydrogenase （LDH）, which is a soluble cytosolic enzyme present in most eukaryotic cells, releases into culture medium upon cell death due to damage of plasma membrane. The increase of the LDH activity in culture supernatant is proportional to the number of lysed cells. ScienCellT LDH Cytotoxicity Assay kit provides a colorimetric method to measure LDH activity using a reaction cocktails containing lactate, NAD+, diaphrose ａnd INT. LDH catalyses the reduction of NAD+ to NADH in the presence of L-lactate, while the formation of NADH can be measured in a coupled reaction in which the tetrazolium salt INT is reduced to a red formazan product. The amount of the highly colored ａnd soluble formazan can be measured at 490 nm spectrophotometrically.

Kit Components

Quality Control

Data from ScienCellT LDH Cytotoxicity Assay of LDH solutions with concentrations ranging from 500 to 7.8 mU/ml shows a linear relationship between OD490nm ａnd LDH concentration （Figure 1）. ScienCellT LDH Cytotoxicity Assay is also applied to Human Astrocytes （HAs） seeded at different densities with （positive control） ａnd without （negative control） Triton X-100 （Figure 2）.

Procedures （96-well plate）

1. Cell Culture setup
   1. Seed cells in a 96-well culture plate in 200 µl of culture medium with or without test compounds. Culture the cells in a CO2 humidified incubator at 37°C for the desired period of time. We recommend that you prepare at least 3 replicates for each test sample. Besides test samples, three positive control cultures in medium with 1% Triton X-100 ａnd three negative control cultures in medium without any test compounds or Triton X-100 should be included.
2. Preparation of LDH standard （optional）
   1. Add 2 µl of LDH stock to 498 µl of PBS to make a 500 µl solution of 1 U/ml LDH.
   2. Obtain 8 test tubes, add 450 µl of culture medium into each tube ａnd label them #1 through #8.
   3. Add 450 µl of the 1 U/ml LDH solution into tube #1 ａnd mix well to get the 500 mU/ml LDH standard.
   4. Transfer 450 µl of the 500 mU/ml LDH standard from tube #1 to tube #2 ａnd mix well to get the 250 mU/ml LDH standard.
   5. Repeat step 4 for tubes #3-7 to serially dilute the LDH standards. Do not add any LDH to tube #8, which serves as the blank.
   6. Obtain a 96-well test plate, prepare 3 replicates （A, B, C） of each LDH standard by aliquoting 150 µl/well of each LDH standard into triplicate wells of the 96-well test plate, according to the following plate format:
      
      

      	#1	#2	#3	#4	#5	#6	#7	#8
      A	500 mU/ml	250 mU/ml	125 mU/ml	62.5 mU/ml	31.8 mU/ml	15.6 mU/ml	7.8 mU/ml	Blank
      B	500 mU/ml	250 mU/ml	125 mU/ml	62.5 mU/ml	31.8 mU/ml	15.6 mU/ml	7.8 mU/ml	Blank
      C	500 mU/ml	250 mU/ml	125 mU/ml	62.5 mU/ml	31.8 mU/ml	15.6 mU/ml	7.8 mU/ml	Blank

3. Preparation of test samples ａnd +/-controls
   1. Centrifuge the 96-well culture plate at 400 g for 5 min ａnd transfer 150 µl of supernatant from each well （test, positive ａnd negative control wells） to the corresponding well of the 96-well test plate.
4. Measurements
   1. To make 60 µl of working reaction mixture for each well of 96-well plate, add 2 µl of sodium lactate, 2 µl of INT ａnd 20 µl of substrate mix to 36 µl of PBS.
   2. Add 60 µl of working reaction mixture into each well of the 96-well test plate containing LDH standard, test samples, or controls. Incubate for 20 minutes at room temperature in dark.
   3. Stop the reaction with 20 µl of sodium oxamate solution per well of 96-well plate.
   4. Read the absorbance at 490 nm with an ELISA plate reader.
5. Calculations
   1. Average the OD490nm of replicate wells of each LDH standard, test sample, control, ａnd blank. Subtract the average OD490nm value of the blank from the average OD490nm values obtained with all other samples.
   2. Based on the calibrated OD490nm of the LDH standard, make a standard curve by plotting OD490nm as a function of LDH concentration. （See Figure 1 for a typical standard curve.） Determine the equation ａnd R2 value of the trend line.
   3. Suppose the equation of the trend line of the standard curve is , calculate the LDH concentration of test samples ａnd controls as follows:
      
      [LDH] = （OD_490nm - B） / A
       
   4. Calculate the cytotoxicity of the test compounds as follows:
      
      Cytotoxicity （%） = （[LDH]_{test sample} - [LDH]_{negative control}） * 100 / （[LDH]_{positive control} - [LDH]_{negative control}）
       
   5. If the exact LDH concentration is not needed, the measurement of the LDH standard curve can be skipped ａnd the relative cytotoxicity of test compounds can also be calculated based on the OD490nm values as follows:
      
      Cytotoxicity （%） = （OD_{490nm, test sample} - OD_{490nm, negative control}） * 100 / （OD_{490nm, positive control} - OD_{490nm, negative control}）

Storage

Store the basal medium at 4oC, the SGS, the FBS ａnd the P/S solution at -20°C. Protect from light.

Shipping

Dry ice.

Reference

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