Parameters Finish: Clear Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Product Name: Palmitoyl Hexapeptide-14 INCI Name: PALMITOYL HEXAPEPTIDE-14 Appearance: White powder Purity: 99% Standard: Enterprise Standard Supplier: ZhenYiBio Palmitoyl hexapeptide-14 is a beauty polypeptide containing six amino acids. This polypeptide has powerful anti-oxidant and anti-aging effects, and can maximize cell regeneration and differentiation. Eliminate wrinkles, fine lines and dark lines can also be largely eliminated. Fatty acid modified peptides can improve the fat solubility of peptides, resist the hydrolysis of intracellular proteases, and promote skin absorption and utilization. Palmitoyl hexapeptide-14 is a compound of alanine, leucine, lysine, phenylalanine residues and palmitic acid. It can stimulate the proliferation of collagen and fibroblasts, stimulate cell migration, and inhibit the activity of MMPs. It is of great significance to support the skin tissue structure and the repair of tissue damage, and can be used for anti-wrinkle, repair and other products.
Parameters Finish: Clear Gloss: N/A Application Methods: Spray Substrate: Rubber, Mango Exposure: Formulation
UV absorbent UV-531 is a kind of anti-aging additives with excellent performance and high efficiency, can absorb 270-340 nm UV light, with light color, non-toxic, good compatibility, small migration, easy to process and other characteristics. It provides maximum protection to the polymer and helps to reduce color, while delaying yellowing and arresting the loss of physical properties. It is widely used in PE, PVC, PP, PS, PC, plexiglass, polypropylene fiber and ethylene vinyl acetate and other aspects. And for the dry phenolic and alkyd varnish, polyurethane, acrylic acid, epoxy and other air-drying products and automobile refit paint, powder coating, polyurethane, rubber products, etc., to provide them with good light stabilization effect. The dosage of 0.1% to 0.5%.
Parameters Finish: Clear Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Parameters Finish: White Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Parameters Finish: Clear Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Parameters Finish: Clear Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Parameters Finish: Clear Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
Parameters Finish: White Gloss: N/A Application Methods: Roller / Brush Substrate: Rubber, Mango Exposure: Formulation
PU Anti-bacterial Wood Polish And Paint PU Sealer Anti-bacterial CATALYST 50% CO15
Uncut Sheet HBsAb Rapid Test Package:30sheets/pouch Specimen:Whole Blood/Serum/Plasma FOR THE QUALITATIVE ASSESSMENT OF HBsAb IN HUMANSERUM, PLASMA OR WHOLE BLOOD INTENDED USE Rapid HBsAb Test is a chromatographic immunoassay for qualitative detection of the surface antibody of hepatitis B virus (Anti-HBs) in human whole blood samples. It is intended for use in medical institution as an aid for diagnosis and management of patients related to infection with hepatitis B as well for screening of blood donors or blood products PRINCIPLE Rapid HBsAb Test employs chromatographic lateral flow device. Colloidal gold conjugated surface antigen reactive to anti-HBs (sAg-Au) are dry-immobilized onto a nitrocellulose membrane strip. When the sample is added, it migrates by capillary diffusion through the strip rehydrating the gold conjugate. If present, anti-HBs will bind with the gold conjugated antigens forming particles. These particles will continue to migrate along the strip until the Test Zone (T) where they are captured by HBsAg immobilized there and a visible red line appears. If there is no anti-HBs in sample, no red line will appear in the Test Zone (T). The gold conjugate will continue to migrate alone until is captured in the Control Zone (C) from immobilized goat, anti-HBs antibody and aggregating in a red line, which indicates the validity of the test STORAGE Store the test device at 4 to 30°C. Do Not Freeze.
INTENDED USE The neisseria gonorrhoeae antigen test card is a rapid visual immunoassay for the qualitative detection of neisseria gonorrhoeae in female endocervical swab and male urethral swab specimens. This kit is intended for use as an aid in the diagnosis of neisseria gonorrhoeae infection. PRINCIPLE The neisseria gonorrhoeae antigen test kit is designed to detect N. Gonorrhoeae through visual interpretation of the color development in the internal strip. The membrane was immobilized with gonococcal Antigen-specific polychonal antibody on the test region (T) and related antibodies on the control region(C). During testing, the specimen is added to the sample region (S) and reacts with anti-gonococcus antibodies conjugated to colored particles and precoated onto the sample pad of the test. Then, the mixture migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient gonococcus antigens in the specimen, a colored band will form at the test region (T) of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
Intended Use The One Step HAV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Hepatitis A Virus (HAV) in Whole Blood /Serum / Plasma to aid in the diagnosis of Hepatitis A Virus. Summary Hepatitis A is an acute, usually self-limiting disease of the liver caused by hepatitis A virus (HAV). HAV is transmitted from person to person, primarily by the faecal-oral route. The incidence of hepatitis A is closely related to socioeconomic development, and seroepidemiological studies show that prevalence of anti-HAV antibodies in the general population varies from 15% to close to 100% in different parts of the world. One step HAV IgG/IgM Test is a simple, visual qualitative test that detects Hepatitis A Virus antibodies in human Whole Blood /Serum / Plasma. The test is based on immunochromatography and can give a result within 15 minutes. Principle The One Step HAV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis A Virus antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing HAV recombinant envelope antigens conjugated with Colloid gold (HAV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-HAV, T2 band is coated with antibody for the detection of IgG anti-HAV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-HAV, if present in the specimen, will bind to the HAV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a HAV IgG positive test result and suggesting a recent or repeat infection. IgM anti-HAV if present in the specimen will bind to the HAV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a HAV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
Specimen:Whole Blood /Serum / Plasma D-Dimer Rapid Test Device is used for the qualitative detection of D-dimer in human whole blood and plasma; The test is used as an aid in the assessment and evaluation of patients with suspected disseminated intravascular coagulation (DIC), deep vein thrombosis (DVT), and pulmonary embolism (PE). During blood coagulation process, fibrinogen is converted to fibrin by the activation of thrombin. The resulting fibrin monomers polymerise to form a soluble gel of non-cross-linked fibrin. This fibrin gel is then converted to cross-linked fibrin by thrombin activated Factor XIII to form an insoluble fibrin clot. Production of plasmin, the major clot-lysing enzyme, is triggered when a fibrin clot is formed. Although fibrinogen and fibrin are both cleaved by the fibrinolytic enzyme plasmin to yield degradation products, only degradation products from cross-linked fibrin contain D-dimer and are called cross-linked fibrin degradation products. Therefore, fibrin derivatives in human blood or plasma containing D-dimer are a specific marker of fibrinolysis. The D-Dimer Rapid Test Device (Whole blood//Plasma) detects D-Dimer through visual interpretation of color development in the internal strip. Anti-D-Dimer antibodies are immobilized on the test region of the membrane, and anti-mouse antibodies immobilized on the control region. During testing, the specimen reacts with anti-D-Dimer antibodies conjugated to colored particles and precoated onto the sample pad of the strip. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient D-Dimer in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
INTENDED USE The One Step RV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Rubella (Virus) in Whole Blood /Serum / Plasma to aid in the diagnosis of RV infection. The test is based on immunochromatography and can give a result within 15 minutes. PRINCIPLE The One Step RV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of RV antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing RV recombinant envelope antigens conjugated with Colloid gold (RV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-RV, T2 band is coated with antibody for the detection of IgG anti-RV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-RV, if present in the specimen, will bind to the RV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a RV IgG positive test result and suggesting a recent or repeat infection. IgM anti-RV if present in the specimen will bind to the RV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a RV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
Owing to its low cost and platy structure, Talc Powder for Paint Industry has gained prominence. Talc is used primarily in industrial paint and coatings, wood lacquers, printing inks, fillers as well as in various coatings. ... Talc increases coverage and weather resistance of the products. The use of talc creates a barri er effect, which limits the penetration of water and corrosive agents into paints and coatings. The Talc Powder for Paint Industry, which we provide, is particularly used in Paints and protective coatings. We provide the Talc Powder for Paint Industry at competitive rates to the clients. The amount of Talc used in paints varies between 2 to 30%. Also the fineness of Talc used in paints varies between 100 to 20. The oil absorption of Talc used in Paints is between 40 to 60 gm per 100 gms House paints, as titanium dioxide extenders to reduce cracking and sagging, and enhance matting. In anti-corrosion primers to improve corrosion resistance and paint adhesion. Features: Mud Cracking Resistance Our Talc's platy particles act as bridges between binder agglomerates and strengthen the paint film. The higher the aspect ratio and particle size of the Talc, the better the mud cracking resistance. Matting Our Talc gives a silky look to paints. Coarse, lamellar talc particles are very efficient matting agents in high PVC paints. Our fine Talc with high surface area can be used to absorb excess binder and give a flattening effect to paints or coatings below critical PVC. High Solids Our double classified, de-dusted Talc with low surface area (low oil absorption) allow a higher filler loading in high solids coatings, resulting in lower VOC emission, lower formulation cost and improved performance at the same time. Barrier Effect The Talc platelets reduce oxygen or water transmission, and protect the binder from UV radiation, thus improving the weather resistance of outdoor paints. Wet scrub resistance Our Talc grades improve the wet scrub resistance of decorative paints, in contrast to Talc containing chlorite (Mg-Al-Silicate), which is not hydrophobic. Anti-corrosive The same barrier effect reduces migration of corrosive agents through steel protective coatings. At the same time, the hydrophobic (unipolar) Talc increases the adhesion of the coating film on the steel substrate, while the platelets improve the mechanical strength of the film.
Zinc Stearate. Zinc Stearate is a zinc soap known for repelling water and is used in the cosmetics and personal care industries as a lubricant. It is an insoluble salt made of commercial stearic acid, a mild fatty acid used as an emollient and lubricant, and is often combined with zinc oxide. Zinc stearate is a â??zinc soapâ?? that is widely used industrially. In this context, soap is used in its formal sense, a metal salt of fatty acid: in this case stearic acid. It is a white solid that repels water. It is insoluble in polar solvents such as alcohol and ether but soluble in aromatic hydrocarbons (e.g., benzene) and chlorinated hydrocarbons when heated. It is the most powerful mold release agent among all metal soaps. It contains no electrolytes and has a hydrophobic effect. Its main application areas are the plastics and rubber industry, where it is used as a releasing agent and lubricant which can be easily incorporated. Zinc Stearate is formed by combining Stearic Acid & Zinc Oxide, the latter of which is an organic white powder compound with a slight characteristic odor. It is insoluble in water, ethyl alcohol & diethyl ether & soluble in acids. In comparison to other metallic stearate, zinc stearate has a low melting point (120 degree C), so it spreads very evenly when heated. Uses and Application of Zinc Stearate- Act as an anti-caking Agent in powdered cosmetics. Act as a lubricant & thickening Agent used to improve texture.. Zinc Stearate is used in plastics and rubber industries, where it is used as a lubricant & release or powdering agent. It functions as an acid scavenger & processes acid in certain Polyolefin applications. It serves as a lubricant acid in sanding sealers and as a flattening agent in paints and coatings. In construction, it is utilized as hydrophobic agents for plasters. In pharmaceuticals & nutraceuticals, it facilitates mould release for tabulating.
Name Of Product - Upscale Vacuum Roll(Size: 15cm*15m) Food Grade, BPA Free, Boil Safe, Microwave Supported, 80+ Micron made of Recyclable Virgin Plastic PE, FDA 21, EN1186 Certified Key Specifications/Special Features - MADE OF 80+ MICRONS THICKENED MATERIAL : The vacuum role is made of 80+ microns thickened material which is tough and durable. It is moisture proof, anti bacterial and suitable for cold storage. Product Keywords - Vacuum Packaging, Vacuum Sealer, Vacuum Rolls, Vacuum Sealing Machine, Vacuum Packaging Machine,
Name Of Product - Upscale Vacuum Roll(Size: 15cm*5m) Food Grade, BPA Free, Boil Safe, Microwave Supported, 80+ Micron made of Recyclable Virgin Plastic PE, FDA 21, EN1186 Certified Key Specifications/Special Features - MADE OF 80+ MICRONS THICKENED MATERIAL : The vacuum role is made of 80+ microns thickened material which is tough and durable. It is moisture proof, anti bacterial and suitable for cold storage. Product Keywords - Vacuum Packaging, Vacuum Sealer, Vacuum Rolls, Vacuum Sealing Machine, Vacuum Packaging Machine,
