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Catalog	name	Description	price
R-PV-048	Tea Polyphenols-Calcium carbonate microsphere（20nm）	Tea Polyphenols-Calcium carbonate microsphere，Adsorption of calcium carbonate microspheres by tea polyphenols，TP-Calcium carbonate microsphere from ruixi.Tea polyphenols, also known as catechins, belong to polyphenols, which are the general term of a group of polyhydroxyphenols contained in tea. Tea polyphenol is a new type of natural antioxidant, whose antioxidant activity is higher than that of non phenolic or mono phenolic hydroxyl antioxidants.	price>
R-M-410	FA-Chitosan	FA-Chitosan,folic acid-Chitosan from ruixi.Chitosan is a biodegradable polymer with low toxicity and good biocompatibility, which is widely used in drug delivery system.Both the single chitosan microspheres and the chitosan composite microspheres can control the release of the drug,improve the stability of the drug,reduce the toxicity of the drug and reduce the harm to human body.	price>
R-M-630	H-Ala-Ala-Ala-OMe acetate salt	H-Ala-Ala-Ala-OMe acetate salt/AAA-OMe, substrate for a simultaneous determination of the esterase and the peptidase activities of pancreatic elastase.	price>
R-R-1785	m-3M3FBS CAS No.200933-14-8	m-3M3FBS/CAS No.200933-14-8 is a potent phospholipase C (PLC) activator. m-3M3FBS stimulates superoxide generation in human neutrophils, upregulates intracellular calcium concentration, and stimulates inositol phosphate generation in various cell lines. m-3M3FBS induces monocytic leukemia cell apoptosis.	price>
R-0412	Ac4GlcNAz	N-azidoacetylglucosamine-tetraacylated，Ac4GlcNAz，Azide modified glucose from ruixi.The tetraacetylated N-Azidoacetyl-glucosamine (Ac4GlcNAz) provides a non-radioactive alternative for glycoconjugate visualization. It is cell-permeable, intracellularly processed and incorporated instead of its natural monosaccharide counterpart N-Acetylglucosamine(GlcNAc).	price>
R-M-411	Kdo Azide	8-Azido-3,8-dideoxy-D-manno-octulosonic acid (Kdo Azide) is an analogue of the natural 3-deoxy-D-manno-octulosonic acid (Kdo) that contains a very small modification, specifically an azido moiety. This molecule can be incorporated by cultured cells (Gram-negative Bacteria, for example) and incorporated into glycans (LPS, for example) during active glycan biosynthesis. Detection utilizes the chemoselective ligation or “click” reaction between an azide and an alkyne or cyclooctyne.Applications:Metabolic Lipopolysaccharide labeling.	price>
R-M-631	H-D-Ala-D-Ala-D-Ala-D-Ala-OH	H-D-Ala-D-Ala-D-Ala-D-Ala-OH(CAS: 926-78-3) is substrate for D-aminopeptidase from Ochrobactrum anthropi.	price>
R-R-1786	Prinaberel CAS No.524684-52-4	Prinaberel (ERB-041)/CAS No.524684-52-4 is a potent and selective estrogen receptor (ER) β agonist with IC50s of 5.4, 3.1 and 3.7 nM for human, rat and mouse ERβ, respectively. Prinaberel displays >200-fold selectivity for ERβ over ERα. Prinaberel is a potent skin cancer chemopreventive agent that acts by dampening the WNT/β-catenin signaling pathway. Prinaberel induces ovarian cancer apoptosis.	price>
R-PRO-001	Fmoc-NH-PEG1-CH2CH2COOH,CAS:1654740-73-4	Fmoc-NH-PEG1-CH2CH2COOH,Fmoc-6-amino-4-oxahexanoic acid from ruixi.Fmoc-N-amido-PEG1-acid is a PEG derivative containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic conditions to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.	price>
R-M-412	PLGA20K-PEG5K-KLWVLPKGGGC	PLGA20K-PEG5K-KLWVLPKGGGC from ruixi.PLGA20K-PEG5K-KLWVLPKGGGC is a polypeptide modified polymer.	price>
R-M-632	H-D-Ala-D-Ala-D-Ala-D-Ala-D-Ala-OH	H-D-Ala-D-Ala-D-Ala-D-Ala-D-Ala-OH,CAS:10491-09-5 from ruixi.It is a polypeptide,the Molecular Formula is C₁₅H₂₇N₅O₆.	price>
R-R-1787	MYCMI-6 CAS No.681282-09-7	MYCMI-6 (NSC354961)/CAS No.681282-09-7 is a potent and selective endogenous MYC:MAX protein interactions inhibitor. MYCMI-6 blocks MYC-driven transcription and binds selectively to the MYC bHLHZip domain with a Kd of 1.6 μM. MYCMI-6 inhibits tumor cell growth in a MYC-dependent manner (IC50<0.5 μM). MYCMI-6 is not cytotoxic to normal human cells. MYCMI-6 induces apoptosis.	price>
R-PRO-002	Fmoc-NH-PEG2-CH2CH2COOH,cas:872679-70-4	Fmoc-NH-PEG2-CH2CH2COOH,Fmoc-9-amino-4,7-dioxanonanoic acid from ruixi. Fmoc-N-amido-PEG2-acid is a PEG derivative containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.	price>
R-M-413	Benzaldehyde-PEG2000-GE11	Peptide GE11 is a small molecule peptide obtained by phage peptide library screening technology,which is composed of 11 amino acids(yhwygytpqnvi).Ge11 can specifically bind to EGFR,and ge11 has no effect on cell growth.The results showed that the liposomes modified with ge11 had high targeting to EGFR.It has been widely used in tumor targeted gene delivery and drug delivery.	price>
R-M-633	H-Ala-Ala-Ala-Tyr-OH	H-Ala-Ala-Ala-Tyr-OH,CAS:112079-60-4 from ruixi.It is a polypeptide , the Molecular Formula is C₁₈H₂₆N₄O₆.	price>
R-R-1788	Taccalonolide A CAS No.108885-68-3	Taccalonolide A/CAS No.108885-68-3 is a microtubule stabilizer, which is a steroid isolated from Tacca chantrieri, with cytotoxic and antimalarial activities. Taccalonolide A causes G2-M accumulation, Bcl-2 phosphorylation and initiation of apoptosis. Taccalonolide A is effective in vitro against cell lines that overexpress P-glycoprotein (Pgp) and multidrug resistance protein 7 (MRP7), with an IC50 of 622 nM for SK-OV-3 cells.	price>
R-PRO-003	Fmoc-NH-PEG3-CH2CH2COOH，cas：867062-95-1	Fmoc-NH-PEG3-CH2CH2COOH,Fmoc-12-amino-4,7,10-trioxadodecanoic acid from ruixi.Fmoc-N-amido-PEG3-acid is a PEG derivative containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.	price>
R-M-414	PPS-Phosphoric acid N=20	PPS-Phosphoric acid N=20,Polyphenylene Sulfide-Phosphoric acid N=20 from ruixi.Polyphenylene sulfide, abbreviated as PPS,is a new type of high performance thermoplastic resin,which has the characteristics of high mechanical strength, high temperature resistance, chemical resistance,fire resistance and good thermal stability.Phosphoric acid group has high binding affinity toward metal oxide surface. Phosphate PEGcan form self-assembly monolayer (SAM) on these surfaces.	price>
R-M-634	H-Ala-Ala-Gln-OH	H-Ala-Ala-Gln-OH(CAS :290312-62-8) is by-product formed during the synthesis of the dipeptide Ala-Gln, glutamine source in parenteral nutrition.	price>
R-R-1789	Piceatannol CAS No.10083-24-6	Piceatannol/CAS No.10083-24-6 is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI). Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties. Piceatannol induces apoptosis in DLBCL cell lines. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells.	price>

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