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Home > ELISA Kit > Researchuse ELISA kit > Agriculture of plant viru...
Plant arginine succinate synthase 1 (ass1) ELISA Kit
Plant arginine succinate synthase 1 (ass1) ELISA Kit Plant arginine succinate synthase 1 (ass1) ELISA Kit Plant arginine succinate synthase 1 (ass1) ELISA Kit
  • Plant arginine succinate synthase 1 (ass1) ELISA Kit

Plant arginine succinate synthase 1 (ass1) ELISA Kit

Item No.: ADL-EL-PT00304
Plant zeatin nucleoside (Zr) ELISA Kit
Plant lutein (carotenol) ELISA Kit
Plant vitamin D (VD) ELISA Kit
Plant growth hormone (GH) kit
Plant glucokinase (GCK) ELISA Kit
  • Specifications:
    48T
    96T
Request Quote PDF Format
Description Common Elisa types Quality control Quality control
Description

Name

Plant arginine succinate synthase 1 (ass1) ELISA Kit

Specifications

96T

article number

HB177-Pt

Species

Plant

Sample type

serum, plasma, tissue homogenate,cell lysate, cell Culture supernatant etc.

Detection range

See the manual for details

Sensitivity

See the manual for details

Response time

1-5h

Sample volume

10ul

Detection wavelength

450nm

Delivery date

3-5 days

Manual

Consult our salesperson for obtaining

Precision
The precision is expressed by the coefficient of variation CV of the measured value of the sample. CV (%) = SD/mean×100
Intra-batch difference: Take the same batch of kits for quantitative detection of low, medium, and high value fixed value samples. Each sample is measured 20 times continuously, and the average value and SD value of samples of different concentrations are calculated.
Inter-batch difference: select 3 different batches of kits to quantitatively determine the low, medium, and high-value fixed value samples. Use the same kit for each sample to repeat the measurement 10 times, and calculate the average value and SD of samples with different concentrations. value6
Intra-run difference: CV<4.3%
Difference between batches: CV<7.5%
Recovery rate
The target protein of known concentration was added to 5 different samples, and the recovery experiment was performed to obtain the recovery range and average recovery rate.

Sample Type

Range (%)

Average Recovery (%)

Tissue Lysates (n=5)

91-108

97

Serum (n=5)

85-107

92

EDTA plasma (n=5)

88-105

94

Cell culture media (n=5)

93-107

96

Linear
Add the target protein of known concentration to     5 samples respectively, do recovery experiment, get the range of recovery rate and average recovery rate. Dilute 5 samples by 2 times, 4 times, 8 times, and 16 times respectively for recovery experiments to obtain the recovery range and average recovery rate.

Sample

1:2

1：4

1:8

1:16

Tissue Lysates (n=5)

92-105%

84-99%

90-102%

80-93%

Serum (n=5)

81-101%

89-99%

86-98%

83-101%

EDTA plasma (n=5)

85-97%

82-101%

83-96%

79-91%

Cell culture media (n=5)

83-105%

89-112%

81-106%

82-110%

 

Specificity
This kit recognizes natural and recombinant Plant arginine succinate synthase 1 (ass1) , and has no obvious cross-reactivity with other similar substances. Due to the limitation of technology and sample source, it is impossible to complete the cross-reaction test of all related or similar substances. Therefore, this kit may have cross-reaction with other untested substances.

Stability
It has been determined that the kit must be stored at the recommended temperature within the validity period, and the activity reduction rate is less than 5%. In order to reduce the influence of external factors on the detection value before and after the destruction of the kit, the environmental conditions of the laboratory should be kept as consistent as possible, especially the temperature, humidity and incubation conditions in the laboratory. Secondly, the operation by the same experimenter can reduce human error.

Kit composition

Serial number

English name

specification

1

Wash solution(30X)

20ml×1 bottle

2

HRP-Conjugate reagent

6ml×1 bottle

3

Microelisa stripplate

12 holes×8 strips

4

Sample diluent

6ml×1 bottle

5

Chromogen Solution A

6ml×1 bottle

6

Chromogen Solution B

6ml×1/bottle

7

Stop solution

6ml×1 bottle

8

Standard

0.5ml×1 bottle

9

Standard diluent

1.5ml×1 bottle

10

Product Description

1 serving

11

Sealing plate membrane

2 sheets

12

Sealing bag

1 piece

Note: Please check whether the label and quantity of the reagents in the kit are consistent with the table before use.
Materials and consumables needed but not provided


1. Microplate reader (it is recommended to warm up the instrument before use)
2. Precise pipettes, tips, and sample tanks
3. Distilled or deionized water
4. Bottle washing or automatic plate washing machine
5. 37℃ water bath or thermostat
6. EP tube
7. Powder-free disposable latex gloves


Storage conditions and validity period
1. Store at 2-8℃, do not freeze, the validity period is 6 months.
2. After opening and use, put the coated microplate into a ziplock bag with desiccant, seal the ziplock bag, and put all reagents back into the refrigerator at 2-8°C.

 

Common Elisa types


ELISA can be used to detect both antigens and antibodies.
Samples to be tested usually include serum, plasma, cell supernatant, tissue homogenate, etc.
Here are three necessary reagents in this assay method:

1. Antigen or antibody on solid phase, ie "immunosorbent"
2. Enzyme-labeled antibodies or antibodies, i.e. "conjugates";
3. Enzyme reaction substrate.

According to the source of the reagent, the nature of the sample, and the  relevant conditions of the detection, a variety of detection methods 
with different purposes can be designed.
Quality control


Strict R&D and verification system to ensure product performance

1.carefully screened pairings
  In the double-antibody sandwich method, capture antibodies and detection antibodies must pass strict screening, and then carry out   scientific concentration adjustment.
2. reliable specificity
   By carefully selecting antibody pairs and optimizing buffers, matrix effects are eliminated and only target analytes are recognized.
3. a variety of experimental principles
   The double-antibody sandwich method, indirect method, and competition method are designed to meet the detection of proxies with  different molecular weights.
4.The sample type has been verified
   It can detect various samples such as serum, plasma, culture supernatant, tissue, etc.
5. Good stability
6. Strict verification tests, including but not limited to the following

a.Intra-panel and inter-panel accuracy
b.Authenticated samples, such as serum, plasma, cell supernatant and other natural sample analysis
c.Blood component interference experiment
d.Linear
e.Recovery rate
f.Reagents and components are stable
These verification processes are reviewed by professional quality assurance personnel to ensure that the test results meet the guidelines and conform to  the established technical specifications.
Quality control


Strict R&D and verification system to ensure product performance

1.carefully screened pairings
  In the double-antibody sandwich method, capture antibodies and detection antibodies must pass strict screening, and then carry out   scientific concentration adjustment.
2. reliable specificity
   By carefully selecting antibody pairs and optimizing buffers, matrix effects are eliminated and only target analytes are recognized.
3. a variety of experimental principles
   The double-antibody sandwich method, indirect method, and competition method are designed to meet the detection of proxies with  different molecular weights.
4.The sample type has been verified
   It can detect various samples such as serum, plasma, culture supernatant, tissue, etc.
5. Good stability
6. Strict verification tests, including but not limited to the following

a.Intra-panel and inter-panel accuracy
b.Authenticated samples, such as serum, plasma, cell supernatant and other natural sample analysis
c.Blood component interference experiment
d.Linear
e.Recovery rate
f.Reagents and components are stable
These verification processes are reviewed by professional quality assurance personnel to ensure that the test results meet the guidelines and conform to  the established technical specifications.
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