|
| 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 |
Diagnostic / Laboratory virus Fluorescence PCR kit Siniperca chuatsi rhabdovirus Nucleic Acid PCR Kit
Intended use:
This kit is suitable for auxiliary diagnosis of Siniperca chuatsi rhabdovirus (SCRV) infection in animal tissue, feed, feces and other samples.
Principle:
This kit to choose a conservative design specific gene probe, the probe can with primer amplification area in the middle of Siniperca chuatsi rhabdovirus (SCRV) 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, thereby quenching groups out of the 3' end, glow, The detection of Siniperca chuatsi rhabdovirus (SCRV) nucleic acid in the completely closed reaction system was realized by fluorescence PCR instrument.
Main components:
| Component | Specification |
| PCR reaction liquid | 24 tubes |
| Positive control | 1 tube |
| Negative control | 1 tube |
1. Sample type
Samples of animal tissue, feed, feces, etc
2. Sample collection and transportation
About 0.1g tissue samples were taken from prawn samples according to different sizes or infection stages. In which, whole individuals were taken from larvae and larvae, head and chest of eyes were removed from juveniles under 3CM, gill area was taken from larger juveniles, and gill filaments or heart or lymphatic organs were taken from adult shrimps.
3. Storage and transportation
Samples are transported in ice bags of 2℃~8℃, and repeated freezing and thawing are prohibited. Short-term storage at -20℃, -70℃ can be long-term storage
PCR amplification and fluorescence detection (PCR detection area):
Put each reaction tube into the PCR instrument and perform PCR amplification according to the following procedures:
| Step | Cycle number | Temperature | Time |
| 1 | 1 | 50℃ | 5min |
| 2 | 1 | 95℃ | 5min |
| 3 | 45 | 95℃ | 10s |
| 60℃ | 30s collect fluorescent |
FAM was selected for detection channel
The results of interpretation:
| Results | Ct Value |
| Positive | Ct≤40 |
| Negative | No Ct value or Ct value=0 |
| 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.
Product performance index:
1. Accuracy
The positive reference materials of testing enterprises were all positive.
2. Minimum detection limit: The detection limit of this kit is 10 copies/μL.
3. Precision: Coefficient of variation (CV,%) of intra-batch precision Ct value is ≤5%.
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.
Operation 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 |
Diagnostic / Laboratory virus Fluorescence PCR kit Siniperca chuatsi rhabdovirus Nucleic Acid PCR Kit
Intended use:
This kit is suitable for auxiliary diagnosis of Siniperca chuatsi rhabdovirus (SCRV) infection in animal tissue, feed, feces and other samples.
Principle:
This kit to choose a conservative design specific gene probe, the probe can with primer amplification area in the middle of Siniperca chuatsi rhabdovirus (SCRV) 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, thereby quenching groups out of the 3' end, glow, The detection of Siniperca chuatsi rhabdovirus (SCRV) nucleic acid in the completely closed reaction system was realized by fluorescence PCR instrument.
Main components:
| Component | Specification |
| PCR reaction liquid | 24 tubes |
| Positive control | 1 tube |
| Negative control | 1 tube |
1. Sample type
Samples of animal tissue, feed, feces, etc
2. Sample collection and transportation
About 0.1g tissue samples were taken from prawn samples according to different sizes or infection stages. In which, whole individuals were taken from larvae and larvae, head and chest of eyes were removed from juveniles under 3CM, gill area was taken from larger juveniles, and gill filaments or heart or lymphatic organs were taken from adult shrimps.
3. Storage and transportation
Samples are transported in ice bags of 2℃~8℃, and repeated freezing and thawing are prohibited. Short-term storage at -20℃, -70℃ can be long-term storage
PCR amplification and fluorescence detection (PCR detection area):
Put each reaction tube into the PCR instrument and perform PCR amplification according to the following procedures:
| Step | Cycle number | Temperature | Time |
| 1 | 1 | 50℃ | 5min |
| 2 | 1 | 95℃ | 5min |
| 3 | 45 | 95℃ | 10s |
| 60℃ | 30s collect fluorescent |
FAM was selected for detection channel
The results of interpretation:
| Results | Ct Value |
| Positive | Ct≤40 |
| Negative | No Ct value or Ct value=0 |
| 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.
Product performance index:
1. Accuracy
The positive reference materials of testing enterprises were all positive.
2. Minimum detection limit: The detection limit of this kit is 10 copies/μL.
3. Precision: Coefficient of variation (CV,%) of intra-batch precision Ct value is ≤5%.
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.
Operation details please check from IFU!
