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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.

  • Monosodium Urate (crystals)

    Biovision | Monosodium Urate (crystals) | 9689

    Monosodium Urate (MSU) is a NLRP3/NALP3 inflammasome activator. Stimulates the caspase-1 activating NLRP3/NALP3 (cryopyrin) inflammasome, resulting in the production of active IL-1β and IL-18. Specially crystallized and tested for biological activity...

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  • MMP-9 Inhibitor

    Biovision | MMP-9 Inhibitor | 1981

    Cell-permeable. A potent, selective, and reversible MMP-9 Inhibitor (IC₅₀ = 5 nM). Inhibits MMP-1 (IC₅₀ = 1.05 µM) and MMP-13 (IC₅₀ = 113 nM) only at much higher concentrations.MMP-9 inhibitor is a potent, selective, and reversible MMP-9 Inhibitor (IC₅₀...

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  • MIF-Antagonist, ISO-1

    Biovision | MIF-Antagonist, ISO-1 | 1895

    Cell-permeable. A macrophage migration inhibitory factor (MIF) antagonist. ISO-1 inhibits MIF pro-inflammatory activities by targeting MIF tautomerase activity. Also inhibits tumor necrosis factor (TNF) release from macrophages isolated from LPS-...

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  • MIF antagonist, p425

    Biovision | MIF antagonist, p425 | 2158

    A counterstain for background autofluorescence in fluorescence and immunofluorescence histochemistry. Acts as an allosteric MIF (macrophage migration inhibitory factor) inhibitor. It occupies an interface of MIF trimers, leading to the loss of its...

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  • Metformin, Hydrochloride

    Biovision | Metformin, Hydrochloride | 1691

    An anti-diabetic agent. It reduces blood glucose levels and improves insulin sensitivity. Its metabolic effects, including the inhibition of hepatic gluconeogenesis, are mediated at least in part by activation of the LKB1-AMPK (AMP-activated protein...

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  • L-JNK Peptide Inhibitor I

    Biovision | L-JNK Peptide Inhibitor I | 7011

    L-JNK Peptide Inhibitor competitively blocks the interaction between JNK and c-Jun, thereby inhibiting the signaling events downstream of JNK, like c-Jun, ATF-2 and ELK1 phosphorylation. To convert JIP-1/IB-1 into cell permeable inhibitors of JNK (JNKI1)...

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  • Leptomycin B

    Biovision | Leptomycin B | 1814

    A potent, specific inhibitor of nuclear export signal (NES)-dependent protein export from the nucleus. It alkylates and inhibits CRM1 (chromosomal region maintenance)/exportin 1(XPO1), a protein required for nuclear export of proteins containing a...

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  • Latrunculin B

    Biovision | Latrunculin B | 2182

    A cell-permeable marine toxin. Disrupts microfilament-mediated processes. Actin polymerization inhibitor in vitro and in vivo by the formation of a 1:1 complex with monomeric G-actin. Depolymerizes actin filaments (F-actin). Less potent than Latrunculin...

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  • Latrunculin A

    Biovision | Latrunculin A | 2181

    A cell-permeable marine toxin. Disrupts microfilament-mediated processes. Actin polymerization inhibitor in vitro and in vivo by the formation of a 1:1 complex with monomeric G-actin. Depolymerizes actin filaments (F-actin) and acts as a phagocytosis...

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  • Lactacystin (Synthetic)

    Biovision | Lactacystin (Synthetic) | 1709

    Cell-permeable. A potent and selective inhibitor of the 20 S proteasome. Binds irreversibly to the active site N-terminal threonine residue of the catalytic β-subunit of the 20S proteasome, thereby inhibiting its chymotrypsin and trypsin-like activities...

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  • Lactacystin (Natural)

    Biovision | Lactacystin (Natural) | 2434

    Cell-permeable. A potent and selective inhibitor of the 20 S proteasome. Binds irreversibly to the active site N-terminal threonine residue of the catalytic β-subunit of the 20S proteasome, thereby inhibiting its chymotrypsin and trypsin-like activities...

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  • EZSolution™ L-685,458

    Biovision | EZSolution™ L-685,458 | 1713

    Cell-permeable. A potent and selective γ-secretase inhibitor (IC₅₀ = 17 nM) .Displays > 50-fold selectivity over a range of aspartyl, serine and cysteine proteases. Exhibits equal potency for inhibition of Aβ40 and Aβ42 peptides (IC₅₀ values are 48 and...

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  • Ingenol 3-angelate

    Biovision | Ingenol 3-angelate | 2593

    Ingenol 3-angelate is a specific Protein Kinase C (PKC) activator and anti-cancer agent. Displays potent antileukemic activity mediated via the d isoform of PKC.Ingenol 3-angelate is a specific Protein Kinase C (PKC) activator and anti-cancer agent...

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  • Ilimaquinone

    Biovision | Ilimaquinone | 2038

    Cell-permeable. A marine sponge metabolite that acts as a cytoplasmic microtubule inhibitor. Induces a complete and reversible breakdown/disruption of Golgi membranes into smaller vesicular structures and blocks the association of the ADP-ribosylation...

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  • IC87114

    Biovision | IC87114 | 1661

    Cell-permeable. A potent, ATP-competitive and selective inhibitor of PI 3-K isoform p110δ (IC₅₀ = 60 nM). Inhibits p110α and p110β only at higher concentrations (>1 µM). IC87114 does not inhibit other PIK-related kinases such as ATM, ATR, DNA-PK, and...

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  • Hh Signaling Pathway Antagonist

    Biovision | Hh Signaling Pathway Antagonist | 1659

    Cell-permeable. A potent antagonist of the Hedgehog (Hh) signaling pathway (IC₅₀ = 70 nM).Hh Signaling Pathway Antagonist is a potent antagonist of the Hedgehog (Hh) signaling pathway (IC₅₀ = 70 nM).Biovision | 1659 | Hh Signaling Pathway Antagonist...

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  • GW 9662

    Biovision | GW 9662 | 1697

    A Potent, selective and irreversible PPARɣ antagonist. Blocks the PPARɣ-induced differentiation of monocytes to osteoclasts by >90% at a dose of 0.1 µM.GW 9662 is a potent, selective and irreversible PPARɣ antagonist. Blocks the PPARɣ-induced...

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  • GSK-3β Inhibitor, TWS119

    Biovision | GSK-3β Inhibitor, TWS119 | 1655

    A potent inhibitor of GSK-3β (Glycogen synthase kinase-3β) (IC₅₀ = 30 nM). At 400 nM, TWS119 induces neurogenesis in murine embryonic stem cells making it a useful tool to regulate stem cell self-renewal and differentiation.GSK-3β Inhibitor, TWS119 is a...

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  • Gö 6976

    Biovision | Gö 6976 | 1711

    Cell-permeable. A potent protein kinase C (PKC) inhibitor (IC₅₀ = 7.9 nM). In vitro, discriminates between Ca²⁺-dependent and -independent isoforms of PKC; selectively inhibits PKCα and PKCβ1 (IC₅₀ values are 2.3 and 6.2 nM respectively) but does not...

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  • GM 6001

    Biovision | GM 6001 | 1799

    Cell-permeable. A broad spectrum matrix metalloprotease (MMP) inhibitor with Ki values of 0.4 nM, 0.5 nM, 27 nM, 3.7 nM, 0.1 nM, 0.2 nM, 3.6 nM, 13.4 nM, 0.36 nM for MMPs -1, -2, -3, -7, -8, -9, -12, -14, and -26, respectively.GM6001 is a broad spectrum...

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  • GF-627368X

    Biovision | GF-627368X | B2029

    GW-627368X is a potent and selective competitive antagonist of the prostanoid EP4 receptor with additional affinity at TP receptors (pKi values are 7.0 and 6.8 in competition radioligand bioassays). Displays antitumor activity.GW-627368X is a potent and...

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  • Fostriecin sodium

    Biovision | Fostriecin sodium | B1241

    Fostriecin is a potent inhibitor of the serine/threonine protein phosphatases PP2A and PP4 with IC₅₀ value of 3.2 and 3 nM, respectively. It also displays weak inhibition of topoisomerase II having IC₅₀ of 40 μM and PP1 with IC₅₀ of 131 μM. Fostriecin...

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  • FK228

    Biovision | FK228 | 2447

    A natural prodrug that inhibits Class I histone deacetylases (HDACs) (IC₅₀ values are: 36, 47, 510 and 14000 nM for HDAC1, HDAC2, HDAC4 and HDAC6, respectively). Displays potent anticancer activities.FK228 is a natural prodrug that inhibits Class I...

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  • FITC-VDVAD-FMK

    Biovision | FITC-VDVAD-FMK | 9498

    FITC-VD(OMe)VAD(OMe)-FMK is a fluorescein isothiocyanate (FITC) conjugate of the cell- permeable caspase-2 inhibitor VD(OMe)VAD(OMe)-FMK that acts as an in situ marker for detection of caspase-2 in living cells. FITC-VD(OMe)VAD(OMe)-FMK is nontoxic, and...

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  • FITC-VAD-FMK

    Biovision | FITC-VAD-FMK | 9497

    FITC-VAD(OMe)-FMK is a fluorescein isothiocyanate (FITC) conjugate of the cell- permeable pan-caspase inhibitor VAD(OMe)-FMK that acts as an in situ marker for detection of caspase in living cells. FITC-VAD(OMe)-FMK is nontoxic, and irreversibly binds to...

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  • FITC-LEHD-FMK

    Biovision | FITC-LEHD-FMK | 9534

    FITC-LE(OMe)HD(OMe)-FMK is a fluorescein isothiocyanate (FITC) conjugate of the cell- permeable caspase-9 inhibitor LE(OMe)HD(OMe)-FMK that acts as an in situ marker for detection of caspase-9 in living cells. FITC-LE(OMe)HD(OMe)-FMK is nontoxic, and...

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  • FITC-IETD-FMK

    Biovision | FITC-IETD-FMK | 9533

    FITC-IE(OMe)TD(OMe)-FMK is a fluorescein isothiocyanate (FITC) conjugate of the cell- permeable caspase-8 inhibitor IE(OMe)TD(OMe)-FMK that acts as an in situ marker for detection of caspase-8 in living cells. FITC-IE(OMe)TD(OMe)-FMK is nontoxic, and...

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  • FITC-DEVD-FMK

    Biovision | FITC-DEVD-FMK | 9499

    FITC-D(OMe)E(OMe)VD(OMe)-FMK is a fluorescein isothiocyanate (FITC) conjugate of the cell- permeable caspase inhibitor D(OMe)E(OMe)VD(OMe)-FMK that acts as an in situ marker for detection of caspase-3 in living cells. FITC-D(OMe)E(OMe)VD(OMe)-FMK is...

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  • FAS Inhibitor, C75

    Biovision | FAS Inhibitor, C75 | 1547

    Inhibitor of fatty acid synthase (FAS) reducing food intake and body weight in mice. Exhibits irreversible slow-binding biphasic inactivation of FAS. Down regulates neuropeptide Y and Agouti-related protein expression. Has been proposed to activiate...

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  • EZSolution™ Y-27632

    Biovision | EZSolution™ Y-27632 | 1784

    A 10 mM (5 mg in 1550 µl) solution of Y-27632, Dihydrochloride (Cat. No. 1596-5) in deionized water.EZSolution™ Y-27632 is a 10 mM (5 mg in 1550 µl) solution of Y-27632, Dihydrochloride (Cat. No. 1596-5) in deionized water.Biovision | 1784 | EZSolution™...

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  • EZSolution™ WP1066

    Biovision | EZSolution™ WP1066 | 2546

    A potent, cell-permeable JAK2 inhibitor. A novel analog of the JAK2 inhibitor AG490 (Cat. No. 1570-5) that blocks STAT3 and phosphoinositide-3-kinase pathways. It is significantly more potent and active against human malignant glioma cells in vitro and...

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  • EZSolution™ Trichostatin A

    Biovision | EZSolution™ Trichostatin A | 2271

    A 10 mM (1 mg in 330 µl) of Trichostatin A (Cat. No. 1606-1) in anhydrous DMSO.Trichostatin A (TSA) is a potent, reversible inhibitor of histone deacetylase.Biovision | 2271 | EZSolution™ Trichostatin A DataSheetAlternate Name/Synonyms: TSA,...

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  • EZSolution™ Tozasertib

    Biovision | EZSolution™ Tozasertib | 1803

    A 100 mM (25 mg in 538.1 µl) solution of Tozasertib (Cat. No. 1595-25) in anhydrous DMSO.EZSolution™ Tozasertib is a 100 mM (25 mg in 538.1 µl) solution of Tozasertib (Cat. No. 1595-25) in anhydrous DMSO.Biovision | 1803 | EZSolution™ Tozasertib...

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  • EZSolution™ Torin 2

    Biovision | EZSolution™ Torin 2 | 2354

    A potent, selective and ATP-competitive mTOR inhibitor (IC₅₀ = 2.1 nM for mTORC1). Torin 2 displays 800-fold selectivity for mTOR over PI3K (cellular EC₅₀ values of 0.25 nM and 200 nM, respectively) and exhibits 100-fold binding selectivity relative to...

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  • EZSolution™ Torin 1

    Biovision | EZSolution™ Torin 1 | 2353

    A potent, selective and ATP-competitive mTOR inhibitor, with IC₅₀ values of 2 and 10 nM for mTORC1 and mTORC2 respectively; Torin1 displays 1000-fold selectivity for mTOR over PI3K (EC₅₀ = 1800 nM) and exhibits 100-fold binding selectivity relative to...

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  • EZSolution™ Torcetrapib

    Biovision | EZSolution™ Torcetrapib | 2533

    Torcetrapib is a cholesteryl ester transfer protein (CETP) inhibitor (IC₅₀ = 37 nM). It raises high-density lipoprotein (HDL) cholesterol and reduces low-density lipoprotein (LDL) cholesterol levels. However, in clinical trials, Torcetrapib displayed...

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  • EZSolution™ Thiazovivin

    Biovision | EZSolution™ Thiazovivin | 1736

    Cell-permeable. A 10 mM (1 mg in 321 µl) solution of Thiazovivin (Cat. No. 1681-1) in anhydrous DMSO.EZSolution™ Thiazovivin is a 10 mM (1 mg in 321 µl) solution of Thiazovivin (Cat. No. 1681-1) in anhydrous DMSO.Biovision | 1736 | EZSolution™...

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  • EZSolution™ Tetrahydrouridine

    Biovision | EZSolution™ Tetrahydrouridine | 2355

    A 100 mM (25 mg in 1007 µl) sterile-filtered solution of Tetrahydrouridine (Cat. No.1671) in H₂O.Tetrahydrouridine is a competitive cytidine deaminase inhibitor and multidrug resistance modulator. Makes tumor cells more sensitive to radiation therapy...

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