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Porcine Circovirus Veterinary Elisa Kit Antibody Fast Detection
Porcine Circovirus type 2 Antibody Diagnostic ELISA Kit for Pig 192 Wells/Kit
1. Porcine Circovirus type 2 Antibody Diagnostic ELISA Kit
Principle
GreenSpring® PCV2 Antibody ELISA Detection Kits are made from
antigen-coated microtiter plates (coated with PCV antigen) and
other reagents. It applies the principle of solid-phase ELISA to
PCV-Ab in serum, and then adds an enzyme conjugate to specifically
bind to the complex of coated antigen + PCV-Ab + enzyme-labeled
anti-pig IgG antibody on the microplate. With TMB substrate, it
produces a certain amount of color. The depth of color is related
to the content of PCV-Ab. When the color value is greater than the
critical value, the pigs are well inoculated or have natural
infection.
2. Porcine Circovirus type 2 Antibody Diagnostic ELISA Kit Components
1 | PCV antigen coated microplate | 96T X 2 | |
2 | Enzyme conjugate | 22ml | yellow lid |
3 | Sample diluent solution | 50ml | transparent lid |
4 | PCV-IgG Negative control serum | 1.5ml | green lid |
5 | PCV-IgG Positive control serum | 1.5ml | red lid |
6 | Substrate | 12ml X2 | orange lid |
7 | Stop solution | 12ml | blue lid |
8 | 20×concentrated washing buffer | 50ml | white lid |
9 | Adhesive Foil | 2 pieces | |
10 | Instruction | 1 piece |
3. Procedure
1. Remove the coated plate (removable) and record the sample
position on the worksheet. Set 2 wells of negative control serum,
add undiluted negative control serum, 2 wells of positive control
serum, add undiluted positive control serum, 100 μL/well. Others
are sample wells, add diluted samples, each 100μL (both single and
double wells) -well test is no problem).
2. Mix gently, cover and incubate at 37°C for 30 minutes.
3. Remove the adhesive foil. Pour the liquid out of the wells,
fully add the diluted wash buffer to each well, and pour out
directly without standing. Repeat 3 times, the last time pat dry on
absorbent paper.
4. Add 100 μL of enzyme conjugate to each well.
5. Cover the board with new adhesive foil. Incubate at 37°C for 30
minutes.
6. Repeat step 3 (washing).
7. Add 100ul of substrate to each well, mix well, and incubate at
37°C for 10 minutes in the dark.
8. Add 50 μL of stop solution to each well, mix gently, and measure
the result.
9. Measure the OD value of each well with a photometer at dual
wavelengths 450nm/630nm.
4. Results
For the assay to be valid, the mean OD value of the positive
control wells must be greater than or equal to 0.6, and the mean OD
value of the negative control wells must be less than 0.1.
Otherwise, the test is invalid and needs to be re-tested.
The result is judged by the S/P value,
S/P=(sample OD450/630- NCx(—))/(PCx(—)- NCx(—)), NCx(—) represents
the average OD450/630 value of the negative control, and PCx(—)
represents the average OD450 of the positive control /630 value
If S/P ≥ 0.2, it is positive; if it is less than 0.2, it is
negative.
5. Product performance
1. Specificity: Use this kit to detect the reference serum, and the
compliance rate reaches 100%.
2. Sensitivity: up to 1:5120.
3. Accuracy: CV(%) is not more than 8%.
4. Stability: 12 months at 2℃~8℃ or 3 days at 37℃, the results can
meet the above three standards.
6. User Notices and Warnings
1. This kit is for research use only.
2. Do not use expired reagents, and do not mix reagents from
different batches.
3. Please read the manual carefully before use.
4. The experimental garbage should be sterilized by high pressure
steam at 121℃ for 30 minutes, or treated with 5.0g/L sodium
hypochlorite disinfectant for 30 minutes and then discarded.
5. Microplates removed from refrigeration should be equilibrated
and allowed to dry at room temperature before opening. Return
unused MicroWell plates to dry foil bags and seal at 4 °C. Unused
liquid reagents should be covered and stored together with other
components at 2-8°C away from light.
6. If the 20X Concentrated Wash Buffer crystallizes, it is a normal
phenomenon, put it at 37℃ to dissolve.
7. Micropipettes should be used to add samples and reagents and
should be frequently demonstrated for accuracy.
8. When adding washing buffer, it should be topped up but not
overflowed to avoid free enzyme or cross-contamination between
wells.
9. The termination solution is corrosive, immediately rinse with
plenty of water when it comes into contact with skin or clothes.
Specifications: 96 holes × 2.
Validity: 12 months.
Storage: 2~8℃, keep away from light.
Production date: on the outer packaging of the kit.
The incubation period of PCV infection is long. Even if it is infected in the embryonic stage or early postnatal stage, the symptoms will appear gradually after weaning. PVC-2 infection can cause the following diseases:
Multiple system failure syndrome after weaning in pigs
It usually occurs in weaned piglets. It was first reported in 1997,
and then reported in America, Europe and Asia. It has been
confirmed that PVC-2 is an important pathogen of post-weaning
multiple system failure syndrome in pigs. The mixed infection and
immune stimulation of reproductive and respiratory syndrome virus,
parvovirus, pseudorabies virus and other pathogens can aggravate
the harm of the disease.
The affected pigs showed poor spirit, poor appetite, slightly high
body temperature, muscle weakness, dysentery, dyspnea, eyelid
edema, jaundice, anemia, emaciation, poor growth and development.
There was a big difference in weight with the same age pigs, skin
eczema, systemic lymph node disease, especially the swelling of
inguinal, mesenteric, bronchial and mediastinal lymph nodes. The
incidence rate was 5% - 30%, and the mortality rate was 5% - 40%,
The convalescent pig becomes a stiff pig.
Dermatitis and nephrotic syndrome
It usually occurs in pigs aged 8-18 weeks. It was first reported in
the United Kingdom in 1993, and then in the United States, Europe,
South Africa and Asia. The incidence rate is 0.15% - 2%, sometimes
as high as 7%. The main symptoms are irregular patches with red and
purple bulges on the perineum and limb skin. The affected pigs
showed subcutaneous edema, loss of appetite, and sometimes
increased body temperature. They usually die within 3 days,
sometimes lasting for 2-3 weeks.
Proliferative necrotizing interstitial pneumonia
This disease mainly harms pigs aged 6-14 weeks. The incidence rate
is 2% - 30%, and the mortality is 4% - 10%.
Reproductive barrier
It leads to an increase in the oestrus rate of sows, mummification,
miscarriage, stillbirth and weak birth.
Q1: When will it be shipped?
A1: We will ship the goods for you as soon as possible within 7
working days after receiving the payment. (In case of external
factors such as the epidemic, the delivery may be delayed)
Q2: Does it support OEM/ODM?
A2: It can be supported, but the specific quantity needs to be more
than 100,000 pieces, which is convenient for customized products.
Q3: How is your factory doing in terms of quality control?
A3: We have nationally certified ISO9001 and ISO13485. Our
production process conforms to standard procedures to ensure
optimum product quality.
Q4: How to provide after-sales service?
A4: We provide professional online technical after-sales service.
We can provide you with one-on-one guidance via video, telephone,
etc.
Q5: What is the payment method?
A5: We receive payment by T/T.
Q6: How to ship?
A6: Choose the best shipping method for you by getting quotes from
our many cooperative carriers, and also ship according to your
requirements.