Soybean leaves are rich in crude protein, crude fat, and are also rich in calcium and phosphorus. Therefore, in the absence of protein feed in rural areas, soybean leaves can be used to feed pigs. There are three specific feeding methods. First, the fresh soybean leaves collected will be freshly removed to remove impurities and foreign matter. After being chopped, they are directly mixed into the pig's diet. The amount of fresh soybean leaves accounts for about one-third of the pig's diet. For piglets under 30 kg, the chopped soybean leaves can be cooked in a pot and fed into the pig's diet. The second is that silage soybean leaves are low in sugar content and rich in protein, suitable for semi-dry silage. The method is: the soybean leaves are air-dried to a moisture content of about 50%, and then rough cut with a knife, and then into a silo, cylinder or plastic silage, compaction seal. Need to use time out of the mix into the pig diet, feeding about 1/4 of the pig diet. Third, the soybean leaves can be placed in a dry and ventilated place by comminution, dried to a moisture content of about 30%, placed in the sun, dried quickly or placed in a drying room to dry, so that the moisture is reduced to less than 10%, and then crushing with a grinder Soybean leaf powder. This powder can be stored for a long time. Pigs can be directly mixed into the pig's diet when they are fed, and their consumption accounts for 20% to 40% of the pig's diet. For soybean leaves used as feed, the best period for collection is the soybean wax ripening period. At this time, not only the soybean leaves are greener, have better nutrition, and have less crude fiber content, but they will not affect the yield and quality of soybeans.
PCR Reagents
PCR Reagents
Real time PCR Kit for Monkeypox Virus is used for in vitro qualitative nucleic acid detection of Monkeypox Virus in Human serum, lesion exudate samples and scab specimens. Primer sets and FAM labeled probes are designed for specific detection of Monkeypox Virus, Human RNase P gene extracted concurrently with the test sample provides an internal control to validate nucleic extraction procedure and reagent integrity. Probe targeting human RNase P gene is labeled with VIC.
Intended Use
The test is intended for in vitro qualitative detection of monkeypox virus
(MPXV) antigen in human oropharyngeal swab, whole blood or skin lesion
materials, including lesion exudate, lesion roofs, lesion crusts.
The test is used for monkeypox virus antigen test of monkeypox suspected
populations. Positive result of the antigen test can be used for early triage and
rapid management of suspected populations, but it cannot be used as
diagnosis basis of monkeypox infection. Negative results do not rule out
monkeypox infection and should not be used as the sole basis for treatment or
patient management decisions. Further nucleic acid detection should be
carried out for suspected population whose antigen test result is positive or
negative.
The test is only for professional use, not suitable for family test. The test result
is only for clinical reference and it is recommended to conduct comprehensive
analysis of the disease condition in combination with clinical manifestations of
patients and other laboratory tests.
Test Principle
According to the gold immunochromatographic test principle, the
nitrocellulose membrane is coated with MPXV mAb 2 and goat anti-mouse IgG
antibody, the gold conjugate pad is labeled with MPXV mAb 1. When the
antigen is contained in the sample, the antigen binds with the corresponding
gold labeled monoclonal antibody to form a compound, moving forward under
the chromatography, then combines with the coated antibody in the test line
to form Au-MPXV mAb 1-antigen-MPXV mAb 2 complex to condense into a red
band (Test line, T), indicating a positive result. When the sample does not
contain antigen, complex cannot be formed in the test line, and no red band
appears, indicating a negative result.
No matter whether the sample contains antigen or not, the gold labeled
monoclonal antibody will combine with the coated goat anti-mouse IgG
antibody at the control line to form a Au-MPXV mAb 1-goat anti-mouse IgG
antibody complex and condense into a red band (Control line,C)
Pcr Reagents,Reagents Used In Pcr,Reagents Required For Pcr,Pcr Reagent Kit
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