MOQ: | We can produce liquid and lyophilized kits |
Price: | USD |
Standard Packaging: | Carton package |
Delivery Period: | Depending on order quantity |
Payment Method: | L/C, T/T, Western Union |
Supply Capacity: | 100,000 per day |
Enterocytozoon hepatopenaei Nucleic Acid Detection Kits
(PCR-Fluorescent Probe Method)
Intended use:
This kit is applied for quarantine inspection of dectecting Enterocytozoon hepatopenaei(EHP) virus before buying larvae in shrimp desalt plant to ensure that larvae do not carry the disease pathogen. Aquaculture enterprises have conducted EHP specific detection on the bottom mud of aquaculture ponds with slow growth of prawn to exclude the hidden danger of liver and intestinal cytiworm parasitization.
Principle:
This kit is chosen infectious subcutaneous and hematopoietic organ necrosis virus (IHHNV) specific fragment to design primers probe probe, the probe with primer amplification area in the middle of a specific binding DNA template, in the process of PCR extension, the circumscribed Taq polymerase enzymes from the 5 'end of fluorescent groups on the probe will be cut down, make it free in the reaction system, Thus, the 3 '-end quenched group was separated and fluorescence was emitted, which was detected by fluorescence PCR instrument to realize the detection of infectious subcutaneous and hematopoietic necrosis virus (IHHNV) in a completely closed reaction system.
Main components:
Component | Specification |
PCR reaction liquid | 24 tubes |
Positive control | 1 tube |
Negative control | 1 tube |
Sample requirements:
1. Sample type
Seedlings: parent, shrimp eggs, seedlings, coarse standard products
Pond: bottom mud, excrement, water body
Bait: live bait, chilled bait and non-high-temperature treated bait samples
2. Transport
Sample collection and transportation shall be carried out in accordance with NY/T 541. Samples shall be transported to the laboratory as soon as possible under refrigerated conditions to avoid repeated freeze-thaw.
3. Sample preservation
It can be stored for 24 hours at 2℃~8℃, and can be stored for a long time at -20℃.
Using Micgene 242/244/244IVD and ABI QuantStudio5:
procedures are set as below:
Steps |
Cycle number |
Temperature | Time |
1 | 1 | 95℃ | 3min |
2 | 45 | 95℃ | 10s |
60℃ |
30sCollect the fluorescent |
FAM was selected for detection channel.
The results of interpretation
Results | Ct Value |
Positive | Ct≤40 |
Negative | No Ct value or Ct value≥45 |
Gray area | 40<Ct<45 |
Note: The result is judged to be grey area, which needs to be rechecked. If the recheck result is Ct value < 45 is considered as positive, and no Ct value or Ct value ≥45 is considered as negative.
Result analysis:
Automatic analysis using instrumentation
Quality control:
Negative control: No obvious amplification curve of FAM detection channel;
Positive control: FAM channel showed obvious amplification curve, Ct value ≤30;
The above conditions are met simultaneously in the same experiment; otherwise, the experiment is invalid and re-testing is required.
Details please check from IFU!
MOQ: | We can produce liquid and lyophilized kits |
Price: | USD |
Standard Packaging: | Carton package |
Delivery Period: | Depending on order quantity |
Payment Method: | L/C, T/T, Western Union |
Supply Capacity: | 100,000 per day |
Enterocytozoon hepatopenaei Nucleic Acid Detection Kits
(PCR-Fluorescent Probe Method)
Intended use:
This kit is applied for quarantine inspection of dectecting Enterocytozoon hepatopenaei(EHP) virus before buying larvae in shrimp desalt plant to ensure that larvae do not carry the disease pathogen. Aquaculture enterprises have conducted EHP specific detection on the bottom mud of aquaculture ponds with slow growth of prawn to exclude the hidden danger of liver and intestinal cytiworm parasitization.
Principle:
This kit is chosen infectious subcutaneous and hematopoietic organ necrosis virus (IHHNV) specific fragment to design primers probe probe, the probe with primer amplification area in the middle of a specific binding DNA template, in the process of PCR extension, the circumscribed Taq polymerase enzymes from the 5 'end of fluorescent groups on the probe will be cut down, make it free in the reaction system, Thus, the 3 '-end quenched group was separated and fluorescence was emitted, which was detected by fluorescence PCR instrument to realize the detection of infectious subcutaneous and hematopoietic necrosis virus (IHHNV) in a completely closed reaction system.
Main components:
Component | Specification |
PCR reaction liquid | 24 tubes |
Positive control | 1 tube |
Negative control | 1 tube |
Sample requirements:
1. Sample type
Seedlings: parent, shrimp eggs, seedlings, coarse standard products
Pond: bottom mud, excrement, water body
Bait: live bait, chilled bait and non-high-temperature treated bait samples
2. Transport
Sample collection and transportation shall be carried out in accordance with NY/T 541. Samples shall be transported to the laboratory as soon as possible under refrigerated conditions to avoid repeated freeze-thaw.
3. Sample preservation
It can be stored for 24 hours at 2℃~8℃, and can be stored for a long time at -20℃.
Using Micgene 242/244/244IVD and ABI QuantStudio5:
procedures are set as below:
Steps |
Cycle number |
Temperature | Time |
1 | 1 | 95℃ | 3min |
2 | 45 | 95℃ | 10s |
60℃ |
30sCollect the fluorescent |
FAM was selected for detection channel.
The results of interpretation
Results | Ct Value |
Positive | Ct≤40 |
Negative | No Ct value or Ct value≥45 |
Gray area | 40<Ct<45 |
Note: The result is judged to be grey area, which needs to be rechecked. If the recheck result is Ct value < 45 is considered as positive, and no Ct value or Ct value ≥45 is considered as negative.
Result analysis:
Automatic analysis using instrumentation
Quality control:
Negative control: No obvious amplification curve of FAM detection channel;
Positive control: FAM channel showed obvious amplification curve, Ct value ≤30;
The above conditions are met simultaneously in the same experiment; otherwise, the experiment is invalid and re-testing is required.
Details please check from IFU!