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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.

  • Gibberellic acid

    Biovision | Gibberellic acid | B2234

    Gibberellic acid (GA) is a tetracyclic di-terpenoid and a plant hormone that stimulates plant growth and development. It stimulates seed germination, triggers transitions from meristem to shoot...

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  • GFT505

    Biovision | GFT505 | B1030

    GFT505 (Elafibranor) is a novel liver-targeted peroxisome proliferator-activated receptor alpha/delta (PPARα/δ) agonist. Displays anti-diabetic effects in db/db mice.GFT505 (Elafibranor) is a novel...

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  • Geodin

    Biovision | Geodin | 9685

    Geodin is a Plasmigen activator inhibitor (PAI-1) inhibitor and Glucose uptake stimulator.Geodin is a Plasmigen activator inhibitor (PAI-1) inhibitor and Glucose uptake stimulator.Biovision | 9685 |...

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  • GDC0994

    Biovision | GDC0994 | B1629

    GDC-0994 is highly selective inhibitor of extracellular signal-regulated kinase (ERK), ERK1 and ERK2, with biochemical potency of 1.1 nM and 0.3 nM, respectively.GDC-0994 is highly selective...

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  • GDC-0980

    Biovision | GDC-0980 | 2668

    GDC-0980, a selective, potent, orally bioavailable inhibitor of Class I PI3 kinase and mTOR kinase (TORC1/2). It inhibits PI3Kα/β/δ/γ with IC₅₀ values of 5 nM/27 nM/7 nM/14 nM, respectively and mTOR...

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  • GDC-0941

    Biovision | GDC-0941 | 1623

    GDC-0941 is a potent inhibitor of p110α and p110δ (IC₅₀ = 3 nM). It selectively binds to PI3K isoforms in an ATP-competitive manner, inhibiting the production of the secondary messenger...

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  • GDC-0917

    Biovision | GDC-0917 | B1918

    GDC-0917 (CUDC-427) is a second mitochondrial activator of caspases (Smac) mimetic, a small molecule inhibitor, that mimics Smac, an endogenous antagonist of IAP proteins. GDC-0917 binds to the Smac...

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  • GDC0879

    Biovision | GDC0879 | B1340

    A novel, potent, and selective inhibitor of B-Raf with an IC50 value of 0.13 nMA novel, potent, and selective inhibitor of B-Raf with an IC50 value of 0.13 nMBiovision | B1340 | GDC0879...

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  • GDC-0853

    Biovision | GDC-0853 | B2074

    GDC-0853 is a potent and selective, Bruton's tyrosine kinase (BTK) inhibitor with potential antineoplastic activity. GDC-0853 suppresses B cell- and myeloid cell-mediated components of disease and...

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  • GDC-0449

    Biovision | GDC-0449 | 1890

    A potent inhibitor of Smoothened (SMO), a key mediator of Hedgehog (Hh) signaling pathway. Inhibition of SMO renders the transcription factor GLI inactive, thus preventing the expression of genes...

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  • GDC-0068

    Biovision | GDC-0068 | 2667

    GDC-0068 is a potent, ATP-competitive, pan-Akt inhibitor with IC₅₀s of 5, 18 and 8 nM for Akt1, Akt2 and Akt3, respectively. Displays selectivity over more than other 200 screened kinases. Potential...

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  • GDC-0032

    Biovision | GDC-0032 | 9573

    GDC-0032 is a potent, and selective inhibitor of Class I PI3-K α, δ, and γ isoforms, with 30-fold less inhibition of the PI3K β isoform relative to the PI3K α isoform. This next generation PI3-K...

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  • GBR-12935

    Biovision | GBR-12935 | B1998

    GBR-12935 is a potent and selective dopamine reuptake inhibitor.GBR-12935 is a potent and selective dopamine reuptake inhibitor.Biovision | B1998 | GBR-12935 DataSheetAlternate Name/Synonyms: 1-(2...

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  • Gardiquimod

    Biovision | Gardiquimod | 2002

    A selective ligand for human or mouse Toll-like receptor 7 (TLR7). Induces the activation of NF-κB in HEK 293 cells expressing TLR7. Activates TLR8 only at high concentrations (3µg/ml). Gardiquimod...

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  • GANT61

    Biovision | GANT61 | 1892

    Cell-permeable. A Hedgehog (Hh) signaling pathway antagonist. Inhibits Hh signaling downstream of Smo and Sufu at the level of Gli (IC₅₀ = 5 µM). GANT61 has also been shown to inhibit the in vitro...

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  • GANT58

    Biovision | GANT58 | 1812

    Cell-permeable. Acts as a blocker of Hedgehog (Hh) pathway downstream of SMO and SUFU causing Gli1 nuclear accumulation. It also targets Gli-mediated gene transactivation (IC₅₀ ~ 5 µM in...

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  • Galloflavin

    Biovision | Galloflavin | 2672

    Galloflavin is a lactate dehydrogenase (LDH) inhibitor inhibiting both LDH-A and LDH-B isoforms of the enzyme with Ki values of 5.46 a µM and 15.06 µM, respectively. It blocks the proliferation of...

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  • Galiellactone

    Biovision | Galiellactone | 2623

    Galiellalactone is a fungal metabolite that inhibits IL-6-mediated JAK/STAT signal transduction in HepG2 cells (IC₅₀ = 0.25-0.5 μM). The selectivity of this compound is achieved by its ability to...

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  • Fusidic acid

    Biovision | Fusidic acid | B2392

    Fusidic Acid is a bacteriostatic antibiotic derived from the fungus Fusidium coccineum that acts as a bacterial protein synthesis inhibitor by preventing the turnover of elongation factor G (EF-G)...

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  • Fusicoccin

    Biovision | Fusicoccin | B1625

    Fusicoccin is a toxin originally extracted from Fusicoccum amygdali DelFusicoccin is a toxin originally extracted from Fusicoccum amygdali DelBiovision | B1625 | Fusicoccin DataSheetAlternate...

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  • FURA-5F/AM

    Biovision | FURA-5F/AM | 9551

    FURA-5F/AM is a fluorescent cell membrane-permeant form of FURA-2 (Cat. No. 2243) that can be loaded into the cell where it is hydrolysed by cytosolic esterases and trapped as the active chelator. ...

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  • FURA-4F/AM

    Biovision | FURA-4F/AM | 9550

    Fura-4F AM is a fluorescent intracellular ratiometric calcium indicator analog of FURA-2 (Cat. No. 2243) for detection of higher Ca²⁺ concentrations. lmax: 370± 3 nm (EtOAc); lem: 475± 4 nm (EtOAc)...

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  • Fucoxanthine

    Biovision | Fucoxanthine | B2072

    Fucoxanthin is a natural pigment found in microalgae, especially diatoms and Chrysophyta. Recently, it has been shown to have antioxidant, anti-inflammatory, anti-tumor, and anti-obesity activity in...

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  • FR180204

    Biovision | FR180204 | B1683

    FR180204 is a potent and selective ATP-competitive inhibitor of ERK1 and ERK2 with Ki value of 0.31 uM and 0.14 uM respectively; has IC50 values of 0.51 and 0.33 μM in enzymatic assays against ERK1...

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  • FPH2(BRD-9424)

    Biovision | FPH2(BRD-9424) | B2267

    FPH2 (BRD-9424) is a potent promoter of differentiation of iPS-derived hepatocytes. FPH2 induces functional proliferation of hepatocytes in vitro, and thus expands mature human primary hepatocytes...

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  • Fosinopril sodium

    Biovision | Fosinopril sodium | B2137

    Fosinopril is the ester prodrug of fosinoprilat, an angiotensin converting enzyme (ACE) inhibitor. In vivo, fosinopril is rapidly hydrolyzed to fosinoprilat in the gastrointestinal mucosa and liver...

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  • Formestane

    Biovision | Formestane | B2041

    Formestane is a steroidal aromatase inhibitor. It binds irreversibly to and inhibits the enzyme aromatase, thereby blocking the conversion of cholesterol to pregnenolone and the peripheral...

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  • FK-866

    Biovision | FK-866 | 1914

    Cell-permeable. FK-866 is a highly specific non-competitive inhibitor of Nicotinamide phosphoribosyltransferase (NAMPT) (Ki = 0.4 nM), causing gradual NAD+ depletion. NAMPT functions as an...

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  • FK-506

    Biovision | FK-506 | 1563

    A potent immunosuppresant and in vitro T cell proliferation blocker. It disrupts calcineurin-mediated signal transduction in T-lymphocytes. It interacts with its FK506-binding protein-12 (FKBP-12),...

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  • FIPI (free base)

    Biovision | FIPI (free base) | B2372

    FIPI is a potent and selective phospholipase D (PLD) inhibitor. FIPI inhibits both PLD1 (IC50 = 25 nM) and PLD2 (IC₅₀ = 20 nM); prevents PLD regulation of F-actin cytoskeleton reorganization, cell...

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  • Filipin III

    Biovision | Filipin III | 2744

    Filipin III is a polyene macrolide antibiotic isolated from Streptomyces filipinensis. It may be used in a double staining procedure for the detection of lipoproteins. Binds specifically to...

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  • FH1 (BRD-K4477)

    Biovision | FH1 (BRD-K4477) | 2732

    FH1 is a small molecule that can enhance the functions of cultured hepatocytes. It enhances differentiation of induced pluripotent stem cells (iPSCs) to hepatocytes and promotes the maturation of...

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  • FG-4592

    Biovision | FG-4592 | 9681

    FG-4592 is an inhibitor of hypoxia inducible factor (HIF) prolyl hydroxylase, potentially useful for the treatment of anemia. FG-4592 stabilizes the activities of HIF, a cytosolic transcription...

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  • Fexaramate

    Biovision | Fexaramate | 9560

    Fexaramate is a potent, selective, non-steroidal, farnesoid X receptor (FXR) agonist.Fexaramate is a potent, selective, non-steroidal, farnesoid X receptor (FXR) agonist.Biovision | 9560 | Fexaramate...

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  • FeTPPS

    Biovision | FeTPPS | 2065

    A peroxynitrite decomposition catalyst. An iron porphyrin complex that catalytically isomerizes peroxynitrite to nitrate both in vivo and in vitro thus serving as a decomposition catalyst and a...

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  • Fatostatin

    Biovision | Fatostatin | 2035

    Cell-permeable. Blocks adipogenesis by inhibiting the activation of SREBPs (Sterol Regulatory Binding Proteins). Inhibits the ER-Golgi translocation of SREBPs via binding to their escort protein...

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  • Fasentin

    Biovision | Fasentin | B1576

    Fasentin is a novel inhibitor of glucose transport that blocks glucose uptake. Fasentin inhibits glucose transport as a mechanism to sensitize cells to death receptor stimuli. Fasentin has been...

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