Seafood like squid, mussels and shellfish shells.
Frozen Yellow Conch, Spider Conch, Scallop Meat And Seashells.
Chinese orange, lemon, australia oranges.
Halal Chicken Sausages, Beef, Chicken, Chicken Sausages, Meat.
Melt-blown fabric BFE: above 95% specification: 25g or 20g width 17.5cm Length: 2900m/roll or customize
This fabric use for protective gowns,baby diapers etc.
The fabrics use for face masks production .
The non woven fabrics most use for face masks , bags, furniture etc.
spunlce nonwovn fabric .We are professional spunlace nonwoven fabric manufacturer in china, feel free to contact me if you are interested in our proudcts.
Variety: dry ginger Product Type: Single Herbs & Spices Drying Process: AD Style: Dried Processing Type: Raw Shape: Piece Color: brown Place of Origin: China Weight (kg): 50 Shelf Life: 24 Brand Name: huaou Model Number: first grade Type: Ginger Taste: Spicy Packing: Customers' Requirements Moisture: 12% Max Application: Food Cooking Storage: Cool Dry Place Appearance: Well-dried Crop: Newest Crop Sample: Avaliable MOQ: 500Kg DELIVERY TIME: Within 7-15 Days Supply Ability
Product name : Ladies Chiffon Dress Detail : pleated and printed Shell : 100%polyester chiffon Lining: 50%viscose 50%polyester jersey MOQ(minimum order quantity): 100 pieces(including the sash for free, mixing different colors/sizes) Unit price: USD$12.5 per piece ( 100 pieces) , USD$10.5 per piece (500 pieces)
detail : pleats and printed shell : 100%polyester chiffon lining: 50%viscose 50%polyester jersey
detail : pleats and printed shell : 100%polyester chiffon lining: 50%viscose 50%polyester jersey
We are a meltblown nonwoven fabric manufacturer .We produce the 95+ rate 25gsm-30gsm 175mm width fabric in a good price.Please contact with me if you are interested in it.Thank you.
We produce the 95+ rate 26gsm-30gsm 175mm fabric in good price.Weclome your contact if you are interested in it.
We produce the 95+ 25gsm-30gsm 175mm fabric in a good price.
The melt-blown non-woven production line can produce PP, PET, ultra-fine fiber non-woven fabrics, focusing on non-woven fabric products with good absorption and high elasticity. The melt-blown non-woven production line runs steadily, with high output and high efficiency, the production of non-woven fabrics has a uniform net, strong strength, good air permeability, non-toxic and odorless, and meets environmental standards.
Commodity: Covid-19 RT-PCR Detection Kit Spec.96 tests/kit Price:FOB SHANGHAI USD3.30/test, USD316.8/kit $3.60/TEST CIF NY AIRPORT OR OTHER MAJOR AIRPORTS USA OR EUROPE OR S. AMERICA OR MIDDLE EAST Payment: T/T ADVANCE 50% BALANCE BEFORE DEPARTURE OR Sight Irrevocable TRANSFERABLE LC Delivery: By AIR, 50days after receipt and confirmation of LC
Sample Types : Including Nasopharyngeal swab, Oropharyngeal swab, Sputum Controls : Internal control, UNG enzyme and dUTP used to reduce risk of contamination, false positive and false negative results Product Information Upper and lower respiratory specimens such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate. Authorized Laboratories Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. About Emergency Use Authorization (EUA) This test (1) has not been FDA cleared or approved, (2) has been authorized by FDA under an EUA for use by authorized laboratories, (3) has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and (4) is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C.360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
The COVID-19 RT-PCR Detection Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C. 263a, to perform high complexity tests. Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper and lower respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infective status. The agent detected may not be the definite cause of disease. Positive results do not rule out bacterial co-infection with other viruses. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The COVID-19 RT-PCR Detection Kit is intended for use by qualified trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR Detection Kit is only for use under the Food and Drug Administration's Emergency Use Authorization. PRINCIPLE OF DETECTION This product is a fluorescent probe-based Taqman RT-PCR assay system. Firstly, the RNA of SARS-CoV-2 will be reverse transcribed into cDNA by reverse transcriptase, and then PCR amplification will be performed with cDNA as template. During amplification of the template, the TaqMan probe will be degraded due to the 5'-3 polymerase activity and exonuclease activity of Taq DNA polymerase, then the separation of fluorescent reporter and quencher enables the fluorescent signal to be detected by instrument. The ORF1ab gene of SARS-CoV-2 will be detected qualitatively by FAM channel, the N gene of SARS-CoV-2 will be detected qualitatively by JOE channel, the E gene of SARS-CoV-2 will be detected qualitatively by ROX channel, and the internal reference will be detected by CY5 channel. dUTP and UNG enzyme are used in the kit to prevent contamination of the amplified products. Internal reference is used in the kit for quality control starting from sample collection
