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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.

  • Biotin-PEG₄-NHS

    Biovision | Biotin-PEG₄-NHS | B1518

    Biotin-PEG₄-NHS is a water-soluble, pegylated reagent for simple and efficient biotin labeling of antibodies, proteins and other primary-amine containing molecules.Biotin-PEG₄-NHS is a water-soluble,...

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  • Biotin-NHS

    Biovision | Biotin-NHS | 2347

    Biotin-NHS is a useful reagent for biotinylation of primary amines under mild conditions (pH~6.5-8.5). Some examples of primary amines for biotinylation include lysines on the surface of proteins,...

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  • Biotin-LC-NHS

    Biovision | Biotin-LC-NHS | 2345

    Biotin-LC-NHS is a useful reagent for biotinylation of primary amines under alkaline conditions (pH~8-9). Some examples of primary amines for biotinylation include lysines on the surface of proteins,...

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  • Biotin-LC-LC-NHS

    Biovision | Biotin-LC-LC-NHS | 2346

    Biotin-LC-LC-NHS is a useful reagent for biotinylation of primary amines under mild conditions (pH~6.5-8.5). Some examples of primary amines for biotinylation include lysines on the surface of...

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  • Biotin-HPDP

    Biovision | Biotin-HPDP | 2329

    KEY FEATURES: • HPDP contains a dithiopyridyl group which is reactive towards sulfhydryl groups (-SH) such as in cysteine (C) side chain to form stable disulfide bond • Contains a spacer arm with a...

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  • BIIB 021

    Biovision | BIIB 021 | 2291

    A synthetic, small molecule Hsp90 inhibitor that binds competitively with geldanamycin in the ATP-binding pocket of Hsp90. In tumor cells, BIIB021 induces the degradation of Hsp90 client proteins...

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  • BIBX-1382

    Biovision | BIBX-1382 | 9463

    BIBX 1382 is a potent, selective, reversible and ATP-competitive inhibitor of EGFR tyrosine kinase (IC₅₀ = 3 nM); displays > 1000-fold lower potency against ErbB2 (IC₅₀ = 3.4 μM) and a range of other...

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  • BIBW2992 (Tovok)

    Biovision | BIBW2992 (Tovok) | 1616

    BIBW-2992 is a potent irreversible EGFR/HER2 inhibitor. The potency of BIBW-2992 on the EGFR and HER2 kinases revealed IC₅₀ values of 0.5 nM and 14 nM, respectively. BIBW-2992 is highly selective for...

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  • BIBS39

    Biovision | BIBS39 | B1071

    BIBS-39 is a novel, nonpeptide angiotensin II receptor antagonist that displays antihypertensive activity. In contrast to the angiotensin II receptor subtype 1 (AT1) selective drug DuP 753, BIBS-39...

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  • BIBF1120

    Biovision | BIBF1120 | 2167

    BIBF1120 is a triple angiokinase inhibitor. It blocks signaling through vascular endothelial growth factor receptors (VEGFR; IC₅₀ values of 13 to 34 nM), platelet-derived growth factor receptors...

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  • BI-2536

    Biovision | BI-2536 | 2370

    BI-2536 is a potent, selective inhibitor of polo-like kinase 1 (PLK1) (IC₅₀ = 0.83 nM). It blocks the activities of Plk2 and Plk3 to a slightly lesser extent with IC₅₀ of 3.5 nM and 9.0 nM,...

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  • BI 6727

    Biovision | BI 6727 | 2222

    A highly potent, selective and ATP-competitive inhibitor of polo-like kinases 1, 2 and 3 (PLK1, 2 and 3), with IC₅₀s at 0.87, 5 and 56 nM, respectively.BI 6727 is a highly potent, selective and...

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  • BGT226

    Biovision | BGT226 | B1719

    BGT226 (NVP-BGT226) is a novel inhibitor of class I PI3K/mTOR with IC50 values of 4 nM, 63 nM and 38 nM for PI3Kα, PI3Kβ and PI3Kγ, respectively.BGT226 (NVP-BGT226) is a novel inhibitor of class I...

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  • BG-45

    Biovision | BG-45 | B1866

    BG-45 is a potent HDAC class I inhibitor with selectivity for HDAC3 (IC₅₀ = 289 nM) over HDAC1, 2. BG45 does not inhibit HDAC6. BG-45 alone or in combination with bortezomib has been shown to...

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  • Berberine Chloride

    Biovision | Berberine Chloride | 1830

    An isoquinoline alkaloid that acts as an anticancer agent. It inhibits cell growth and induces apoptosis in a variety of cancer cell lines. It induces the most potent apoptosis in acute lymphoblastic...

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  • Bempedoic acid

    Biovision | Bempedoic acid | B1913

    Bempedoic acid is an ATP citrate lyase (ACL) inhibitor. ACL is an enzyme involved in fatty acid and cholesterol synthesis. Bempedoic acid is a convenient, oral, once-daily LDL-C lowering drug that...

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  • BEC

    Biovision | BEC | 2359

    A potent, slow-binding competitive inhibitor of recombinant rat liver arginase I with a Ki of 0.4-0.6 µM. It is also a potent inhibitor of human arginase II with Ki values of 0.31 µM and 30 nM at pH...

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  • Beauvericin

    Biovision | Beauvericin | B1246

    Beauvercin is an enniatin mycotoxin isolated from fungus Beauveria sp. It has shown cytotoxic properties against insect cells SF-9 and induces apoptosis with IC₅₀ value of 4.5 µM. It has shown to...

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  • BDA366

    Biovision | BDA366 | B1827

    BDA-366 is a small-molecule Bcl2-BH4 domain antagonist, that binds BH4 with high affinity and selectivity. BDA-366-Bcl2 binding induces conformational change in Bcl2 that abrogates its antiapoptotic...

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  • BBT-594

    Biovision | BBT-594 | B2114

    BBT-594 is a potent and selective RET and JAK2 inhibitor. It impairs GDNF-RET signaling and GDNF-dependent growth of MCF7-LTED cells. Displays potent anticancer activity.BBT-594 is a potent and...

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  • BAZ2-ICR

    Biovision | BAZ2-ICR | B1865

    BAZ2-ICR is a small molecule inhibitor of BAZ2A (Kd = 109 nM; IC₅₀ = 130 nM) and BAZ2B (Kd = 170 nM; IC50 = 180 nM) bromodomains. It displays 15-fold selectivity for binding BAZ2A/B over CECR2 and...

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  • BAY-1217389

    Biovision | BAY-1217389 | B1295

    BAY-1217389 is a potent, and selective inhibitor of the serine/threonine kinase monopolar spindle 1 (Mps1, TTK), with potential antineoplastic activity. Upon administration, BAY-1217389 selectively...

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  • BAY 85-3934

    Biovision | BAY 85-3934 | 9597

    Molidustat (BAY-85-3934) is a novel inhibitor of hypoxia-inducible factor (HIF) prolyl hydroxylase (PH) which stimulates erythropoietin (EPO) production and the formation of red blood cells without...

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  • BAY 80-6946

    Biovision | BAY 80-6946 | B1267

    BAY 80-6946 is a highly selective and potent pan-class I PI3K inhibitor with sub-nanomolar IC₅₀s against PI3Kα and PI3Kδ. BAY 80-6946 displays preferential inhibition (about 10-fold) of AKT...

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  • BAY 63-2521

    Biovision | BAY 63-2521 | 2644

    BAY 63-2521 is a potent activator of soluble guanylate cyclase (sGC).BAY 63-2521 is a potent activator of soluble guanylate cyclase (sGC).Biovision | 2644 | BAY 63-2521 DataSheetAlternate...

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  • BAY 57-1293

    Biovision | BAY 57-1293 | 2556

    BAY 57-1293 is a potent helicase primase inhibitor. It inhibits replication of herpes simplex virus (HSV) type 1 and type 2 in the nanomolar range in vitro by abrogating the enzymatic activity of the...

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  • BAX Activator, BAM7

    Biovision | BAX Activator, BAM7 | 2451

    A potent and selective BAX activator (EC₅₀ = 3.3 μM). BAM7 directly binds at the BH3-binding site; selective for BAX over other antiapoptotic and proapoptotic proteins. BAM7 triggers in vitro BAX...

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  • BAR-502

    Biovision | BAR-502 | B1965

    BAR-502 is a dual FXR (farnesoid X receptor) and GPBAR1 (G protein-coupled bile acid-activated receptor) agonist. BAR-502 promotes browning of white adipose tissue and reverses liver steatosis and...

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  • BAR-501

    Biovision | BAR-501 | B1591

    BAR-501 is a selective GPBAR1 agonist devoid of any FXR agonistic activity. It effectively transactivates GPBAR1 in HEK293 cells overexpressing a CRE along with GPBAR1, with an EC₅₀ of 1 μM. Exposure...

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  • BAPTA AM

    Biovision | BAPTA AM | 2242

    A cell-permeable, selective chelator of intracellular calcium stores. BAPTA is105-fold greater affinity for Ca2+ than for Mg2+. Inhibits thapsigargin-induced apoptosis in rat thymocytes.BAPTA AM is a...

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  • BAG 956

    Biovision | BAG 956 | 2456

    A potent, ATP-competitive, dual PI3K/PDK-1 inhibitor in vitro and in vivo (IC₅₀ = 56, 444, 34, 117 and 240 nM for PI3K p110-α ,β,d, γ, and PDK1 kinases, respectively). Displays anticancer properties...

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  • Bacitracin

    Biovision | Bacitracin | B1529

    Bacitracin is a peptide antibiotic and an inhibitor of peptidoglycan synthesis. Inhibits bacterial cell wall synthesis by inhibiting dephosphorylation of lipid pyrophosphate. Bacitracin is used to...

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  • Azidothymidine

    Biovision | Azidothymidine | B1113

    Azidothymidine is a nucleoside reverse transcriptase inhibitor that, following triphosphorylation by thymidine kinase, potently blocks replication of HIV (EC₅₀ = 3 nM) with low cytotoxicity (CC₅₀ > 5...

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  • AZD-9291 mesylate

    Biovision | AZD-9291 mesylate | B1899

    AZD9291 is a potent, selective, and irreversible, third generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI). It inhibits EGFR phosphorylation in EGFR-bearing cells...

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