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Reagents

A substance which is used as a chemical reaction or it is a test reactions occurs. A reagents is to measure the chemical substance is present or not because reagents is the components or a mixture. A chemical reagents works like a detectives which charged and point out the other substance in chemical reactions. For making a reagents the equal number of volumes solutions A and B use immediately and then it is used as a reagents.1.5g of ferric chloride and 2.0g of potassium thiocynate in 100 ml water to dissolve after that make saturated solution in 50% ethnol.

The reagents take action when solvents involved in the reaction which are usually called reactants but catalysts are not consumed with the reactions hence they are not reactants. Iodine is not soluble in water therefore the iodine reagents is made in dissolving the water with a helps of potassium iodide.

  • Timentin

    Biovision | Timentin | B1508

    Timentin is a mixrure (15:1) of Ticarcillin Disodium Salt/Potassium Clavulanate. It acts as a β-Lactamase inhibitor. Highly effective combination against gram negative bacteria such as Agrobacterium strains.Timentin is a mixrure (15:1) of Ticarcillin...

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  • Tiliroside

    Biovision | Tiliroside | 1879

    A naturally occurring flavonoid that shows anti-complement, anti-inflammatory and free radical scavenger activity. Inhibits the production of the inflammatory mediators nitric oxide (NO), TNF-α and IL-12 in activated macrophages. Also inhibits human Low...

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  • Tie2 Kinase Inhibitor

    Biovision | Tie2 Kinase Inhibitor | B1338

    Tie2 kinase inhibitor is a potent and selective Tie2 inhibitor with IC50 of 0.25 ΜmTie2 kinase inhibitor is a potent and selective Tie2 inhibitor with IC50 of 0.25 mΜBiovision | B1338 | Tie2 Kinase Inhibitor DataSheetAlternate Name/Synonyms:...

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  • Ticarcillin Disodium

    Biovision | Ticarcillin Disodium | B1536

    Ticarcillin is a β-lactam antibiotic with a broad spectrum of bactericidal activity against many gram-positive and gram-negative aerobic and anaerobic bacteria. It is commonly used in combination with clavulanate in order to improve its efficacy. A...

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  • THZ1 hydrochloride

    Biovision | THZ1 hydrochloride | 9544

    THZ1 is a potent, cell-permeable, and selective covalent CDK7 inhibitor (IC₅₀ = 3.2 nM) that preferentially diminishes transcription in cancer cells. It displays unprecedented ability to target a remote cysteine residue located outside of the canonical...

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  • THZ1 (Free base)

    Biovision | THZ1 (Free base) | 9664

    THZ1 is a potent, cell-permeable, and selective covalent CDK7 inhibitor (IC₅₀ = 3.2 nM) that preferentially diminishes transcription in cancer cells. It displays unprecedented ability to target a remote cysteine residue located outside of the canonical...

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  • Thymoquinone

    Biovision | Thymoquinone | B2172

    Thymoquinone is a natural phytochemical that displays anti-inflammatory properties, blocking the synthesis of leukotrienes. It inhibits the growth of leukemia cells (IC₅₀= 1.5 μg/ml), inducing apoptosis by down-regulating the expression of Bcl-2 while...

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  • Thioridazine Hydrochloride

    Biovision | Thioridazine Hydrochloride | B1581

    Thioridazine is a dopamine receptor antagonist that displays antipsychotic activity. It suppresses several types of cancer and has specificity for leukemia stem cells. Also displays potent antitumor effects on lung cancer stem-like cells.Thioridazine is...

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  • Thio-NAD

    Biovision | Thio-NAD | 9483

    An analog of NAD. Use of Thio-NAD instead of NAD (Cat. No. 2734) as a substrate for NAD(+)-consuming enzymes is more advantageous since the reduced form of Thio-NAD exhibits a substantial increase in absorbance at 405 nM, the most commonly available...

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  • Thiocolchicine

    Biovision | Thiocolchicine | 2213

    An antimitotic alkaloid. Tubulin polymerization and microtubule assembly inhibitor and axonal cytoskeleton modulator; apoptosis inducer. Thiocolchicine-dimers were shown to be potent topoisomerase I inhibitors.Thiocolchicine is an antimitotic alkaloid...

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  • TGR5-Receptor-Agonist

    Biovision | TGR5-Receptor-Agonist | B1635

    TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell assay (pEC50 = 6.8) and in melanophore cells (pEC50 = 7.5).TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell...

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  • TGR-1202

    Biovision | TGR-1202 | B1284

    TGR-1202 (also known as RP5264), is a highly specific inhibitor of PI3Kδ, targeting the δ isoform with nanomolar potency and several-fold selectivity over the α, β, and g isoforms of PI3K.TGR-1202 (also known as RP5264), is a highly specific inhibitor of...

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  • TG101348

    Biovision | TG101348 | 2314

    TG101348 is a potent, and selective inhibitor of JAK2 (IC₅₀ = 3 nM). It has a 35- and 334-fold selectivity over JAK3 and JAK1, respectively.TG101348 is a potent, and selective inhibitor of JAK2 (IC₅₀ = 3 nM). It has a 35- and 334-fold selectivity over...

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  • TG100713

    Biovision | TG100713 | B1717

    TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ.TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ.Biovision | B1717 | TG100713 DataSheetAlternate Name/Synonyms: TG100713; TG100713; TG 100713;...

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  • Tetrandine

    Biovision | Tetrandine | B2089

    Tetrandrine is a bisbenylisoquinoline alkaloid that displays very broad pharmacological actions, including anti-tumor activity. It enhances the cytotoxicity of MDR-related drugs via modulation of P-gp. Also acts as a calcium channel blocker.Tetrandrine...

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  • Tetracycline Hydrochloride

    Biovision | Tetracycline Hydrochloride | B1535

    Tetracycline is a broad-spectrum antibiotic that prevents bacterial growth by inhibiting protein synthesis. It binds to a single site in the 30S ribosomal subunit which prevents attachment of aminoacyl tRNA to the ribosomal acceptor site. It is used in...

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  • Terpendole C

    Biovision | Terpendole C | 2214

    Isolated from Albophoma yamanashiensis. An acyl-CoA:cholesterol acyltransferase (ACAT) isozymes ACAT1 and ACAT2 inhibitor. Also acts as a tremorgen and cholesteryl ester (CE) synthesis inhibitor.Terpendole C is an acyl-CoA:cholesterol acyltransferase...

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  • Tenofovir disoproxil fumarate

    Biovision | Tenofovir disoproxil fumarate | 1920

    A water-soluble diester prodrug of the active ingredient Tenofovir, that belongs to a class of antiretroviral drugs known as nucleotide analogue reverse transcriptase inhibitors (NtRTIs), which block reverse transcriptase, an enzyme crucial to viral...

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  • TD-139

    Biovision | TD-139 | B2266

    TD-139 is a potent, synthetic inhibitor of galectin-3. TD-139 has high affinity for galectin-3 with a Kd of 14 nM and 10 nM for galectin-1, but low affinity for galectins 2, 4N, 4C, 7, 8N, or 9NTD-139 is a potent, synthetic inhibitor of galectin-3...

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  • TCS-359

    Biovision | TCS-359 | B2212

    TCS-359 is a potent, ATP-competitive inhibitor of FLT3 receptor tyrosine kinase (IC₅₀ = 42 nM) that displays selectivity over a range of other kinases. It blocks the proliferation of myelomonocytic leukemia MV4-11 cells. TCS-359 synergistically increases...

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  • TCS OX2 29

    Biovision | TCS OX2 29 | B1838

    TCS OX2 29 is a potent and selective OX2 (Orexin-2) receptor antagonist (IC₅₀ = 40 nM). Displays >250-fold selectivity for OX2 over OX1 (Orexin-1) and >50 receptors, ion channels and transporters.TCS OX2 29 is a potent and selective OX2 (Orexin-2)...

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  • TC-S 7010

    Biovision | TC-S 7010 | B1203

    TC-S 7010 is a potent and selective inhibitor of Aurora kinase A (IC₅₀ = 3.4 nM). It displays1000-fold selectivity for Aurora kinase A over Aurora kinase B. Displays antiproliferative activity in HCT116 and HT29 cells (IC₅₀ values are 0.19 and 2.9 μM...

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  • TCID

    Biovision | TCID | 2204

    Cell-permeable. A potent and selective inhibitor of ubiquitin C-terminal hydrolase L3 (UCH-L3) (IC50 = 0.6 µM). Inhibits ubiquitin C-terminal hydrolase L1 (UCH-L1) only at higher concentrations (IC50 = 75 µM).TCID is a potent and selective inhibitor of...

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  • TC-H 106

    Biovision | TC-H 106 | B1148

    TC-H 106 is a class I Histone deacetylase (HDAC) inhibitor with IC₅₀ values of 150,370,760 and 5000 nM for HDAC1, 3, 2 and 8 respectively. TC-H 106 shows slow and tight binding inhibitory activity on class I HDACs and does not show inhibitory effect on...

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  • TCEP.HCl

    Biovision | TCEP.HCl | 1202

    A water-soluble, odorless, thiol-free reagent useful for the selective reduction of disulfides. Compared to DTT, TCEP is more stable, more effective and able to reduce disulfide bonds at lower pHs.TCEP. HCl is a 1 M solution of TCEP. HCl (Cat. No. 1202)...

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  • TC-E 5003

    Biovision | TC-E 5003 | B1177

    TC-E 5003 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor (IC₅₀ = 1.5 μM); displays no inhibitory activity against CARM1 and Set7/9 methyltransferases. Inhibits growth of MCF7a breast cancer cells and LNCaP prostate cancer cells...

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  • Taurocholic acid sodium salt

    Biovision | Taurocholic acid sodium salt | 2829

    Taurocholic acid sodium is a bile acid conjugate with detergent properties. This anionic detergent is useful for the solubilization of lipids and membrane-bound proteins.Taurocholic acid sodium is a bile acid conjugate with detergent properties. This...

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  • TASIN-1 hydrochloride

    Biovision | TASIN-1 hydrochloride | B2088

    TASIN-1 (Truncated APC Selective INhibitor-1) is a novel truncated APC selective inhibitor, selectively killing colorectal cancer cells that express truncated APC by reducing cellular cholesterol levels and inducing apoptotic cell death through the ER...

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  • TAS-120

    Biovision | TAS-120 | B2354

    TAS-120 is a novel, potent and highly selective FGFR inhibitor that irreversibly inhibits all four FGFR subtypes at nanomolar concentrations. It blocks the phosphorylation of FGFRs and impedes downstream signaling pathways in cells. TAS-120 prevents the...

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  • Tanshinone IIA-Sulfonic Sodium

    Biovision | Tanshinone IIA-Sulfonic Sodium | B1902

    Sodium tanshinone IIA sulphonate (T06) is a water-soluble derivative of tanshinone IIA, that displays versatile biological properties. Recently, it has been shown to act as an ectosteric inhibitor of cathepsin K (CatK). T06 binds in an ectosteric side of...

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  • Talabostat mesylate

    Biovision | Talabostat mesylate | B2061

    Talabostat is a nonselective inhibitor of post-proline cleaving serine proteases. The inhibition of the highly related cytosolic serine proteases Dpp8 and Dpp9 (Dpp8/9) by Val-boroPro was recently demonstrated to trigger an immunostimulatory form of...

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  • TAK-700

    Biovision | TAK-700 | B2209

    TAK-700 is a potent and highly selective human 17,20-lyase inhibitor (IC₅₀ = 38 nM). Displays >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). Displays antiandogen activity.TAK-700 is a potent and highly selective human...

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  • TAK-063

    Biovision | TAK-063 | B1067

    TAK-063 is a highly potent, cell-permeable PDE10A inhibitor (IC₅₀ = 0.30 nM) with excellent selectivity (>15000-fold selective over other PDEs).TAK-063 is a highly potent, cell-permeable PDE10A inhibitor (IC₅₀ = 0.30 nM) with excellent selectivity...

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  • TAK 165

    Biovision | TAK 165 | 1951

    Cell-permeable. A potent inhibitor of the human epidermal growth factor receptor 2 (HER2) tyrosine kinase (IC₅₀ = 6 nM). Displays > 4000-fold selectivity over EGFR, FGFR, PDGFR, JAK1 and Src. TAK 165 inhibits bladder, kidney and androgen-independent...

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  • TAE-226

    Biovision | TAE-226 | 9436

    TAE-226 is a potent ATP-competitive inhibitor of FAK and IGF-IR with potential anticancer activity. TAE-226 can block FAK and IGF-IR signaling pathways. TAE-226 inhibits the phosphorylation of FAK as well as the downstream effectors AKT, extracellular...

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  • T-705 (Favipiravir)

    Biovision | T-705 (Favipiravir) | 2778

    T-705 (Favipiravir) is an antiviral drug that selectively inhibits the RNA-dependent RNA polymerase of influenza virus. It is phosphoribosylated by cellular enzymes to its active form, favipiravir-ribofuranosyl-5'-triphosphate (RTP). Favipiravir is...

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  • T5601640

    Biovision | T5601640 | B1097

    T5601640, also known as T56-LIMKi, has high specific inhibitory activity for LIMK2 and shows little or no activity with LIMK1. It decreases levels of phosphorylated coflin (p-coflin) inhibiting several cancer cell lines including those of pancreatic...

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  • Syrosingopine

    Biovision | Syrosingopine | B1323

    Syrosingopine is an inhibitor of the vesicular monoamine transporters. Recently, it has been shown that the anticancer activity of the widely used diabetic drug metformin is strongly potentiated by syrosingopine. Syrosingopine sensitizes cancer cells to...

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  • SYK Inhibitor, R406

    Biovision | SYK Inhibitor, R406 | 9682

    R406 is a potent SYK (Spleen Tyrosine Kinase) inhibitor (IC₅₀ = 41 nM). R406 strongly inhibits SYK but not Lyn, and displays 5-fold less potency towards FLT3. R406 induces apoptosis in diffuse large B-cell lymphoma cell lines. It blocks B cell receptor...

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  • Syk Inhibitor

    Biovision | Syk Inhibitor | 1983

    Cell-permeable. An oxindole derivative that acts as a potent, reversible, and ATP-competitive Spleen tyrosine kinase (Syk) inhibitor (IC₅₀ = 14 nM). Has been shown to effectively inhibit FcεRI-mediated degranulation in the rat basophilic leukemia cell...

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  • SYBR Green I

    Biovision | SYBR Green I | B1747

    SYBR Green I is a highly sensitive fluorescent DNA binding stain for staining of double stranded DNA (dsDNA) or oligonucleotides in agarose or polyacrylamide gels.SYBR Green I is a highly sensitive fluorescent DNA binding stain for staining of double...

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  • SW-044248

    Biovision | SW-044248 | B1135

    SW-044248 is a selective Topoisomerase I inhibitor. It is extremely potent and selectively toxic to NSCLC killing ~15% of a 74 NSCLC cell lines. It was not toxic to immortalized human bronchial cell lines. The intense transcriptional response to...

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  • SW-033291

    Biovision | SW-033291 | 9584

    SW-033291 is a potent inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH) (Ki = ~0.1 nM). It rapidly increases the levels of PGE2 in bone marrow and other tissues in mice after intraperitoneal injection. SW033291 accelerates hematopoietic...

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  • Suramin Hexasodium Salt

    Biovision | Suramin Hexasodium Salt | 1874

    A P2x and P2y purinergic receptor antagonist that displays antitumor, antiangiogenic and antiparasitic activities. Inhibits sirtuin 1, sirtuin 5 and topoisomerase II. Inhibits the cell surface binding of various growth factors including PDGF, EGF, FGFa...

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  • Suplatast tosylate

    Biovision | Suplatast tosylate | 2624

    Suplatast tosylate is a Th2 cytokine inhibitor and an immunomodulator. It suppresses eosinophil infiltration, IgE production, and allergic inflammation by suppressing the production of IL-4 and IL-5 . Displays antiasthmatic, anti-inflammatory and...

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  • Sunitinib, Free base

    Biovision | Sunitinib, Free base | 2097

    Sunitinib is a free base form of Sunitinib malate (Cat. No. 1611).Sunitinib is a free base form of Sunitinib malate (Cat. No. 1611).Biovision | 2097 | Sunitinib, Free base DataSheetAlternate Name/Synonyms: SU-11248, Sutent, PHA-290940AD,...

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  • Sunitinib Malate (Sutent)

    Biovision | Sunitinib Malate (Sutent) | 1611

    Sunitinib is a potent inhibitor of CSF-1 receptor kinase in an enzyme assay, with an IC₅₀ of 7 nM, and inhibits receptor phosphorylation in a cellular assay with an IC₅₀ of 61 nM. Sunitinib inhibits SCF-induced phosphotyrosine levels on KIT (IC₅₀ = 1 -...

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  • Sulfo-SMCC

    Biovision | Sulfo-SMCC | 2320

    KEY FEATURES: • Amine reactive Sulfo-NHS ester that crosslinks efficiently with primary amine-containing molecules • Has a maleimide functional group that can be utilized to react specifically with cysteines or sulfhydryl (-SH) groups • Water-soluble;...

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  • Sulfo-SANPAH

    Biovision | Sulfo-SANPAH | 2324

    KEY FEATURES & APPLICATIONS: • It contains an NHS ester that reacts with primary amines and a nitrophenylazide group that is photoreactive at 320-350 nm • Non-cleavable and irreversible • Membrane-impermeable • Amine-reactive; has a spacer arm...

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  • Sulfo-NHS-SS-Biotin

    Biovision | Sulfo-NHS-SS-Biotin | 2323

    KEY FEATURES: • Sulfo-NHS-SS-Biotin is amine-reactive and • Has a long chain spacer arm (24.3 Å) separating the biotin group from the amino-reactive sulfo-NHS ester • Water-soluble; can be used under physiologic conditions • It is possible to cleave...

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