Description
Lactate Dehydrogenase (LDH) Activity Assay Kit
Note: Take two or three different samples for prediction before test.
Operation Equipment: Spectrophotometer/microplate reader
Cat No: BC0685-100T/48S
Size:100T/48S
Components:
Extract solution: 60 mL×1. Storage at 4℃;
Reagent I: 7 mL×1. Storage at 4℃.
Reagent II: powder×1. Storage at -20℃. Working solution: dissolve with 1.3 mL of distilled water before
use. It can be divided into tubule after matching, which can be preserved for two weeks at -20℃. Avoid
repeated freeze and thaw cycles.
Reagent III: 7 mL×1. Storage at 4℃.
Reagent IV: 25 mL×1. Storage at 4℃.
Sodium pyruvate standard solution: 1 mL (2 μmol/mL) ×1. Storage at 4℃.
Product Description:
Lactate dehydrogenase (LDH or LD) is the terminal enzyme of the glycolysis pathway which is found in
nearly all living cells (animals, plants, and prokaryotes). LDH catalyzes the conversion of lactate to
pyruvic acid and back, as it converts NAD+
to NADH and back.
NAD+
and lactic acid are oxidized to pyruvic acid by the catalysis of LDH. Pyruvate further reacted with
2,4-dinitrophenylhydrazide to form pyruvate dinitrobenzone, which show brown red color in alkaline
solution and the color depth is proportional to the concentration of pyruvate.
Reagents and Equipment Required but Not Provided:
Spectrophotometer/Microplate reader, thermostat water bath, desk centrifuge, adjustable pipette, micro
glass cuvette/96 well flat-bottom plate, mortar/homogenizer, ice, distilled water.
Procedure:
I. Sample preparation:
1. Bacteria、cells or tissue sample:
Bacteria or cells:
Collecting bacteria or cells into the centrifuge tube. The liquid in the upper layer is discarded after
centrifugation. The ratio of bacteria/cell amount (104
): Extract solution volume (mL) is 500~1000:1(it is
suggested to take about 5 million bacteria/cell and add 1 mL of Extract solution). Bacteria and cell is split
by ultrasonic (placed on ice, 200W, work time 3s, interval 10s,repeat for 30 times). Centrifuge at 8000
rpm 4℃ for 10 minutes, take the supernatant and put it on ice for test.
Tissue:
Ice-bath homogenate is conducted according to the ratio of tissue mass (g): Extract solution volume (mL)
= 1: 5~10 (it is suggested to take about 0.1 g of tissue and add 1 mL of Extract solution). Ice bath
homogenization. Centrifuge at 8000 rpm and 4℃ for 10 minutes, take the supernatant and put it on ice for
test.
2. Serum (plasma) sample:
Detect sample directly.
Procedure:
- Preheat the Spectrophotometer/Microplate reader 30 minutes, adjust wavelength to 450 nm, set zero with distilled water.
- Sodium pyruvate standard solution: take 100 μL of standard solution, dilute to 1, 5, 0.25, 0.125, 0
μmol/mL, and use 2, 1, 0.5, 0.25, 0.125, 0 μmol/mL as standard curve.
- Sample Test
Reagent name (μL) | Test tube(At) | Control tube(Ac) | Standard tube(As) |
Sample | 10 | 10 | – |
Standard Solution | – | – | 10 |
Reagent I | 50 | 50 | 50 |
Reagent II | 10 | – | – |
Distilled water | – | 10 | 10 |
Mixed thoroughly, incubate at 37℃(mammal) or 25℃(other species) water bath for 15 minutes. | |||
Reagent III | 50 | 50 | 50 |
Mixed thoroughly, incubate at 37℃(mammal) or 25℃(other species) water bath for 15 minutes. | |||
Reagent IV | 150 | 150 | 150 |
Mixed thoroughly, place at room temperature for 3 minutes. Take 200 μL of reaction solution in micro glass cuvette/96 well flat-bottom plate, measured the absorbance at 450 nm, ΔA=AT-AC. Each test tube should set a control tube.
III. LDH Calculations
1. Sample Sodium pyruvate content
2. Set the standard curve, y-axis as the standard concentration, μmol/mL, x-axis as the 450 nm
absorption. Put ΔA(x) into standard curve, calculate y (μmol/mL)
3. Serum (plasma) sample LDH activity
Unit definition: One unit of enzyme activity is defined as the amount of enzyme catalyzes the producing of
1 nmol of pyruvic acid per minute every milliliter of serum.
LDH(U/mL)=y÷T×103=66.7×y
4. Tissue, bacteria or cultured cells LDH activity
A. Protein concentration:
Unit definition: One unit of enzyme activity is defined as the amount of enzyme catalyzes the producing of
1 nmol of pyruvic acid per minute every milligram of protein.
LDH(U/mg prot)= y÷T÷Cpr×103 =66.7×y÷Cpr
B. Sample weight
Unit definition: One unit of enzyme activity is defined as the amount of enzyme catalyzes the producing of 1 nmol of pyruvic acid per minute every gram of tissue.
LDH(U/g)= y÷T÷W×103=666.7×y
C. Cell amount
Unit definition: One unit of enzyme activity is defined as the amount of enzyme catalyzes the producing of 1 nmol of pyruvic acid per minute every 10000 cells.
LDH(U/104cell)= y÷T÷500×103=0.133×y
Vs: Supernate volume (mL), 0.01 mL;
Vsv: Extract solution volume, 1 mL;
T: Reaction time, 15 minutes;
Cpr: Sample protein concentration, mg/mL;
W: Sample weight, 0.1 g;
500: Total number of bacteria or cells, 5 million;
103: 1 μmol/mL=103 nmol/mL.
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