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| Product | Description | |
|---|---|---|
| CAPS | 100g Pack Size. Group: Buffers. Formula: C9H19NO3S. CAS No. 1135-40-6. Prepack ID 24971012-100g. Molecular Weight 221.32. See USA prepack pricing. |  |
| CAPS | 500g Pack Size. Group: Buffers. Formula: C9H19NO3S. CAS No. 1135-40-6. Prepack ID 24971012-500g. Molecular Weight 221.32. See USA prepack pricing. | |
| CAPS | CAPS, cyclohexylaminopropane sulfonic acid, is a surfactant. CAPS can be used as biological buffer (0.05 M, pH 11) for dialysis [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: N-Cyclohexyl-3-aminopropanesulfonic acid. CAS No. 1135-40-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-D0869. |  |
| Capsaicin | 1g Pack Size. Group: Aroma Chemicals, Diagnostic Raw Materials, Research Organics & Inorganics, Testing Standards. Formula: C18H27NO3. CAS No. 404-86-4. Prepack ID 31397045-1g. Molecular Weight 305.41. See USA prepack pricing. | |
| Capsaicin | Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin has pain-relieving, antioxidant, anti-inflammatory, anti-cancer and certain neurotoxic effects [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (E)-Capsaicin. CAS No. 404-86-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-10448. | |
| Capsaicin | Capsaicin - Product ID: NST-10-110. Category: Alkaloids. Alternative Names: Adlea, Ausanil, Axsain, Capsaicine, Capsicin, Dolenon, Mioton, Ovocap, Qutenza, Zostrix. Purity: 98%. Test method: HPLC. CAS No. 404-86-4. Pack Sizes: 1g, 2g, 5g, 10g. Appearance: Off-white to yellowish Powder. Molecular formula: C18H27NO3. Mole weight: 305.41. Storage: +2 +8 °C. |  |
| Capsaicin | It is used as a tool in neurobiological research. Prototype vanilloid receptor agonist. Topical analgesic. Group: Biochemicals. Alternative Names: (6E)-N-[(4-Hydroxy-3-methoxyphenyl)methyl]-8-methyl-6-nonenamide; trans-8-Methyl-N-vanillyl-6-nonenamide; Axsain; Mioton; Zacin; Zostrix. Grades: Highly Purified. CAS No. 404-86-4. Pack Sizes: 50mg. US Biological Life Sciences. |  Worldwide |
| Capsaicin, (6E)- | Capsaicin, (6E)-. Group: Biochemicals. CAS No. 404-86-4. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Capsaicin 99+% (GC) | Capsaicin 99+% (GC). Group: Biochemicals. Grades: GC. CAS No. 404-86-4. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Capsaicin-d3 | Capsaicin-d3. Group: Biochemicals. Alternative Names: (6E)-N-[(4-Hydroxy-3-methoxy-d3-phenyl)methyl]-8-methyl-6-nonenamide; trans-8-Methyl-N-vanillyl-6-nonenamide-d3; Axsain-d3; Mioton-d3; Zacin-d3; Zostrix-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Capsaicin ≥97% (Single peak, HPLC) | Capsaicin ≥97% (Single peak, HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 404-86-4. Pack Sizes: 100mg, 250mg, 25mg, 1g. US Biological Life Sciences. | Worldwide |
| Capsaicin (Standard) | Capsaicin (Standard) is the analytical standard of Capsaicin. This product is intended for research and analytical applications. Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin has pain relief, antioxidant, anti-inflammatory, neuroprotection and anti-cancer effects [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (E)-Capsaicin (Standard). CAS No. 404-86-4. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-10448R. | |
| Capsaicin USP | 8-Methyl-N-vanillyl-trans-6-nonenamide. Afrazine. Grades: USP. CAS No. 404-86-4. Product ID: 8-01375. Molecular formula: C18H27NO3. Mole weight: 305.41. Source : MFCD No. MFCD00017259. |  |
| Capsanthin | analytical standard. Group: Colorant standardschiral molecules. |  |
| Capsanthin | Capsanthin. Group: Biochemicals. Alternative Names: Red Chilli Color/ capsanthin; (3R,3'S,5'R)-3,3'-Dihydroxy- β,κ-caroten-6'-one; (all-E)-9-(4-Hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16,18-Nonadecanonaen-1-one; all-trans-Capsanthin. Grades: Highly Purified. CAS No. 465-42-9. Pack Sizes: 10g. Molecular Formula: C40H56O3, Molecular Weight: 584.87. US Biological Life Sciences. | Worldwide |
| Capsanthin | Capsanthin. Group: Nano fabric coatings. Alternative Names: 2-[(Dimethylamino)Methyl]-4-[2-[(1E)-3-(1,1-Dimethylethoxy)-3-Oxo-1-Propenyl]Phenyl]-1,4-Dihydro-6-Methyl-3,5-Pyridinedicarboxylic Acid Diethyl Ester. CAS No. 465-42-9. Product ID: (2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one. Molecular formula: 584.9. Mole weight: C40H56O3. CC1=C (C (C[C@@H] (C1)O) (C)C)/C=C/C (=C/C=C/C (=C/C=C/C=C (\C)/C=C/C=C (\C)/C=C/C (=O)[C@@]2 (C[C@H] (CC2 (C)C)O)C)/C)/C. 99.9%. |  |
| capsanthin/capsorubin synthase | This multifunctional enzyme is induced during chromoplast differentiation in plants. Isomerization of the epoxide ring of violaxanthin gives the cyclopentyl-ketone of capsorubin or capsanthin. Group: Enzymes. Synonyms: CCS; ketoxanthophyll synthase; capsanthin-capsorubin synthase. Enzyme Commission Number: EC 5.3.99.8. CAS No. 162032-85-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5516; capsanthin/capsorubin synthase; EC 5.3.99.8; 162032-85-1; CCS; ketoxanthophyll synthase; capsanthin-capsorubin synthase. Cat No: EXWM-5516. |  |
| Capsazepine | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. | |
| Capsazepine | Capsazepine, a benzazepine derivative, has been found to be a sensory neurone excitotoxin that could be used against hyperalgesic responses. IC50: 562 nM (Rat TRPV1). Uses: Capsazepine has been found to be a sensory neurone excitotoxin that could be used against hyperalgesic responses. Synonyms: N-[2-(4-Chlorophenyl)ethyl]-1,3,4,5-tetrahydro-7,8-dihydroxy-2H-2-benzazepine-2-carbothioamide. Grades: > 95%. CAS No. 138977-28-3. Molecular formula: C19H21ClN2O2S. Mole weight: 376.91. |  |
| Capsazepine | Capsazepine. Group: Biochemicals. Grades: Purified. CAS No. 138977-28-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Capsazepine - CAS 138977-28-3 | A competitive antagonist of Capsaicin and resiniferatoxin. Capsazepine (1 μM) blocks capsaicin (60 nM) stimulated firing of C-fibers. Group: Fluorescence/luminescence spectroscopy. | |
| Capsazepine (N-[2-(4-Chlorophenyl)ethyl]-1,3,4,5-tetrahydro-7,8-dihydroxy-2H-2-benzazepine-2-carbothioamide) | A selective vanilloid receptor antagonist (Ki=3.2uM). Group: Biochemicals. Alternative Names: N-[2-(4-Chlorophenyl)ethyl]-1,3,4,5-tetrahydro-7,8-dihydroxy-2H-2-benzazepine-2-carbothioamide. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| CAPS, Free Acid | CAPS is a buffer solution used to increase the sensitivity of the detention of sulfite in flow injection procedure. Group: Biochemicals. Alternative Names: 3-(Cyclohexylamino)-1-propanesulfonic Acid; 3- (Cyclohexylamino) propanesulfonic Acid; Cyclohexylaminopropane sulfonic Acid; WAS-12. Grades: Molecular Biology Grade. CAS No. 1135-40-6. Pack Sizes: 100g, 250g, 500g, 1Kg. Molecular Formula: C9H19NO3S, Molecular Weight: 221.32. US Biological Life Sciences. | Worldwide |
| Capsiamide | Capsiamide is a long chain amide found in essential oil of Capsicum (all hot pepper varieties). Studies showed that Capsiamide decreased spontaneous motor activity and produced a significant prolongation of sleeping time after sodium pentobarbital. Group: Biochemicals. Alternative Names: N- (13-Methyltetradecyl) acetamide; Cap-A; Capsi-amide. Grades: Highly Purified. CAS No. 64317-66-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Capsiate | analytical standard. Group: Flavor and fragrance standards. | |
| Capsiate | A TRPA1 and TRPV1 Channel Activator. Group: Biochemicals. Alternative Names: (6E)-8-Methyl-6-nonenoic acid (4-hydroxy-3-methoxyphenyl)methyl ester, 4-Hydroxy-3-methoxybenzyl (E)-8-methyl-6-nonenoate, Vanillyl (E)-8-methyl-6-nonenoate. Grades: Highly Purified. CAS No. 205687-01-0. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C18H26O4, Molecular Weight: 306.4. US Biological Life Sciences. | Worldwide |
| Capsiate | Capsiate, as a capsaicin analogue extracted from a non-pungent cultivar of CH-19 sweet red pepper, is an orally active agonist of TRPV1 [1]. Uses: Scientific research. Group: Natural products. CAS No. 205687-01-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N8377. | |
| Capsiconiate | Capsiconiate is a coniferyl ester that has been isolated from certain plants in the Solanaceae family, including plants in the genus Capsicum. It is a TRPV1 agonist, non-selective cation and calcium permeable channel. Like capsaicin, capsiconiate is an agonist of the transient receptor potential vanilloid receptor TRPV1 (EC50 = 3.2 μM). But the maximum response induced by capsiconiate through TRPV1 is only 20% of that of capsaicin. Synonyms: Coniferyl (E)-8-methyl-6-nonenoate. Grades: ≥98%. CAS No. 946572-73-2. Molecular formula: C20H28O4. Mole weight: 332.4. | |
| Capsicum Extract | Capsicum Extract. Applications: Capsicum extract(capsaicin) is widely used in medicine, military and chemical industry. natural capsaicin production are mainly used in the reseach and development of medicine, by its powerful effect of relieve pain. Group: Others. Purity: Capsaicin 95%. Source: Chili Pepper, dicotyledonous plants, one year or perennial herbaceous plants, native to tropical South America, the late Ming dynasty was introduced into China. There are spicy, for food. Chili grown in mild climate , like water. Chili contain rich vitamin C, beta-carotene, folic acid, magnesium and potassium; Capsaicin in capsicum also has anti-inflammatory and antioxidant effect. Vitamin C content in chili ranks first in the vegetables. Capsicum Extract; Capsicum annuum Linn. Cat No: EXTC-177. | |
| Capsicum oleoresin 60% | 5g Pack Size. Group: Analytical Reagents, Aroma Chemicals, Biochemicals, Building Blocks, Flavours and Fragrance Materials. Formula: N/A. CAS No. 8023-77-6. Prepack ID 90025463-5g. See USA prepack pricing. | |
| Capsicum Oleoresin High Pungency | Capsicum Oleoresin High Pungency. CAS No. 8023-77-6. FEMA No. 2234. Kosher: Y. VIGON Item # 501219. Categories: Speciality Ingrdients Suppliers, Flavors. |  America & Internationally |
| Capsimycin | Capsimycin is an antifungal antibiotic produced by Streptomyces sp. C 49-87. It has antifungal activity, especially against Phytophthora capsici. CAS No. 70694-08-5. Molecular formula: C30H40N2O6. Mole weight: 524.65. | |
| CAPSO | 100g Pack Size. Group: Biochemicals, Buffers. Formula: C9H19NO4S. CAS No. 73463-39-5. Prepack ID 90030068-100g. Molecular Weight 237.32. See USA prepack pricing. | |
| CAPSO | 500g Pack Size. Group: Biochemicals, Buffers. Formula: C9H19NO4S. CAS No. 73463-39-5. Prepack ID 90030068-500g. Molecular Weight 237.32. See USA prepack pricing. | |
| CAPSO | CAPSO is a biological zwitterionic buffer with the useful pH range from 8.9 to 10.3 [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 73463-39-5. Pack Sizes: 10 g; 25 g. Product ID: HY-D0870. | |
| Capso 99+% | Capso 99+%. Group: Biochemicals. Alternative Names: 3-(Cyclohexylamino)-2-hydroxy-1-propanesulphonic acid. Grades: Reagent Grade. CAS No. 73463-39-5. Pack Sizes: 25g, 100g, 250g, 1Kg. Molecular Formula: C9H19NO4S, Molecular Weight: 237.32. US Biological Life Sciences. | Worldwide |
| Capsorubin | Capsorubin. Group: Biochemicals. Alternative Names: (3S,3'S,5R,5'R)-3,3'-Dihydroxy-κ,κ-carotene-6,6'-dione; (1R,1R,4S,4S)-(all-E)-1,20-Bis(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16,18-eicosanonaene-1,20-dione; Capsorubin; all-trans-Capsorubin. Grades: Highly Purified. CAS No. 470-38-2. Pack Sizes: 5mg. Molecular Formula: C40H56O4, Molecular Weight: 600.87. US Biological Life Sciences. | Worldwide |
| CAPSO Sodium salt | 100g Pack Size. Group: Buffers. Formula: C9H18NO4SNa. CAS No. 102601-34-3. Prepack ID 41933774-100g. Molecular Weight 259.3. See USA prepack pricing. | |
| CAPSO Ultrapure | 100g Pack Size. Group: Biochemicals, Buffers. Formula: C9H19NO4S. CAS No. 73463-39-5. Prepack ID 11091556-100g. Molecular Weight 237.32. See USA prepack pricing. | |
| CAPS Sodium salt | 100g Pack Size. Group: Buffers. Formula: C9H18NO3SNa. CAS No. 105140-23-6. Prepack ID 65152663-100g. Molecular Weight 243.3. See USA prepack pricing. | |
| Capstone® FS-30 | Capstone® FS-30. Uses: Designed for use in research and industrial production. Appearance: Liquid. CAS No. 1640092-35-8. Density: 1.1 g/mL at 25 °C. Product ID: ACM1640092358. Alfa Chemistry ISO 9001:2015 Certified. |  |
| capsular-polysaccharide endo-1,3-α-galactosidase | Hydrolyses the galactosyl-α-1,3-D-galactose linkages only in the complex substrate, bringing about depolymerization. Group: Enzymes. Synonyms: polysaccharide depolymerase; capsular polysaccharide galactohydrolase. Enzyme Commission Number: EC 3.2.1.87. CAS No. 62213-16-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3951; capsular-polysaccharide endo-1,3-α-galactosidase; EC 3.2.1.87; 62213-16-5; polysaccharide depolymerase; capsular polysaccharide galactohydrolase. Cat No: EXWM-3951. | |
| capsular-polysaccharide-transporting ATPase | ABC-type (ATP-binding cassette-type) ATPase, characterized by the presence of two similar ATP-binding domains. Does not undergo phosphorylation during the transport process. An enzyme that exports capsular polysaccharide from Gram-negative bacteria. Group: Enzymes. Enzyme Commission Number: EC 3.6.3.38. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4676; capsular-polysaccharide-transporting ATPase; EC 3.6.3.38. Cat No: EXWM-4676. | |
| Capsule essence mixing bottle | This package is a professional light bottle to avoid direct sunlight, and it can be used longer after opening. Product ID: PM-071. Category: Double cavity mixed one bottle. Product Keywords: Cosmetic Plastic Packaging; Capsule essence mixing bottle; PM-071; Double cavity mixed one bottle;. Administration route: Total height: 113mm, straight diameter: 28mm, pump output: 0.23CC,cover material: AS/PCTG,Pump head material: PP, bottle material: AS/PCTG. |  |
| 01-A-Metals-37mm spiked cassette capsules | 01-A-Metals-37mm spiked cassette capsules. Uses: For analytical and research use. Group: Environmental proficiency testing. Catalog: APS003845. Format: 4 x 37 mm diameter cellulose acetate "cassette capsule" spiked with metal solutions plus 2 x blank capsules. | |
| 0.5% DiI Encapsulated DOTAP Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. |  |
| 0.5% DiI Encapsulated DOTMA Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% DiO Encapsulated DOTAP Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% DiO Encapsulated DOTMA Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DC-Chol:DOPE (1:2) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DC-Chol:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DDAB:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DDAB:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DDAB Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DOTAP:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DOTAP:Chol:DOPE (10:75:5) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DOTAP:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DOTMA:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated DOTMA:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% NBD-DOPE Encapsulated GL-67:DOPE (1:2) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DC-Chol:DOPE (1:2) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DC-Chol:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DDAB:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DDAB:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DDAB Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DOTAP:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DOTAP:Chol:DOPE (10:75:5) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DOTAP:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DOTMA:Chol (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| 0.5% Rhod-PE Encapsulated DOTMA:DOPE (50:50) Liposomes | Cationic liposomes are used for the delivery of genetic materials such as various types of DNA and RNA. In order to capture more plasmid efficiently, the negative charge of pDNA is neutralized with positive charge of cationic lipids due to electrostatic interaction and deliver them into cells. So they are researched for use as delivery vectors in gene therapy. Uses: Cancer research; target delivery. Group: Cationic liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
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