Shop by Category

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, pegylated reagent for simple and efficient biotin...

    NULL320.00 - NULL1,024.00
    Choose Options
  • Biotin-PEG₄-amine

    Biovision | Biotin-PEG₄-amine | 2791

    KEY FEATURES: • Polyethylene glycol (PEG) groups in spacer arm enhances water solubility of biotinylated molecules • Spacer arms providing slightly different options for controlling steric hindrance and hydrophilicity • Water-soluble; can be used...

    NULL386.00 - NULL1,271.00
    Choose Options
  • 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, antibodies, etc.Biotin-NHS is a useful reagent for...

    NULL182.00 - NULL7,022.00
    Choose Options
  • 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, antibodies, etc. Inserts a 6-atom spacer between...

    NULL222.00 - NULL1,516.00
    Choose Options
  • 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 proteins, antibodies, etc. Inserts a 14-atom spacer between...

    NULL303.00 - NULL11,200.00
    Choose Options
  • 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 length of 29.2 Å that prevents steric hindrance to...

    NULL501.00 - NULL1,696.00
    Choose Options
  • 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 including HER-2, AKT, and Raf-1 and up-regulates...

    NULL222.00 - NULL616.00
    Choose Options
  • 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 related tyrosine kinases (IC₅₀ > 10 μM).BIBX 1382 is a...

    NULL288.00 - NULL894.00
    Choose Options
  • 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 these kinases and no additional inhibition of other...

    NULL329.00 - NULL935.00
    Choose Options
  • 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 also displays affinity for the angiotensin II receptor...

    NULL271.00 - NULL828.00
    Choose Options
  • 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 (PDGFR; IC₅₀ values of 59 to 65 nM), and fibroblast growth...

    NULL205.00 - NULL2,200.00
    Choose Options
  • 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, respectively. BI-2536 potently causes a mitotic arrest and...

    NULL271.00 - NULL795.00
    Choose Options
  • 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 ATP-competitive inhibitor of polo-like kinases 1, 2 and 3...

    NULL190.00 - NULL501.00
    Choose Options
  • 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 PI3K/mTOR with IC50 values of 4 nM, 63 nM and 38 nM for...

    NULL239.00 - NULL533.00
    Choose Options
  • 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 dose-dependently inhibit tumor growth in a mouse model of...

    NULL239.00 - NULL697.00
    Choose Options
  • BF2649 hydrochloride

    Biovision | BF2649 hydrochloride | B2279

    BF2649 is a potent, cell-permeable and selective histamine H3 receptor inverse agonist (EC₅₀ = 1.5 nM, Ki = 0.16 nM). BF2649 displays nootropic effects in cognitive disorders; reduces locomotor hyperactivity induced by methamphetamine.BF2649 is a potent,...

    NULL288.00 - NULL894.00
    Choose Options
  • Bexgliflozin (EGT1442)

    Biovision | Bexgliflozin (EGT1442) | B1929

    Bexagliflozin is a potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitor with IC₅₀ values of 5.6 µM and 2 nM for human SGLT1 and SGLT2, respectively. Bexagliflozin dose-dependently reduces HbA(1c) and blood glucose concentration without...

    NULL222.00 - NULL631.00
    Choose Options
  • Bestatin hydrochloride

    Biovision | Bestatin hydrochloride | 9630

    Bestatin is a competitive protease inhibitor that inhibits aminopeptidase B, leukotriene A4 hydrolase, aminopeptidase N. It displays no inhibition of aminopeptidase A, trypsin, chymotrypsin, elastase, papain, pepsin, or themolysinBestatin is a...

    NULL239.00 - NULL697.00
    Choose Options
  • 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 leukemia (ALL) cells with both MDM2 overexpression and...

    NULL182.00 - NULL418.00
    Choose Options
  • Berbamine dihydrochloride

    Biovision | Berbamine dihydrochloride | 2520

    Berbemine is a naturally occurring alkaloid that displays several biological properties. Berbamine potently suppresses liver cancer cell proliferation and induces cancer cell death by targeting Ca²⁺/calmodulin-dependent protein kinase II (CAMKII). Also...

    NULL205.00 - NULL567.00
    Choose Options
  • Bendamustine Hydrochloride

    Biovision | Bendamustine Hydrochloride | B1596

    Bendamustine is a novel alkylating agent with a benzimidazole ring giving it purine analogue-like properties. Like other alkylating agents, bendamustine is thought to act by modifying and cross linking purine bases in DNA, thus inhibiting DNA, RNA and...

    NULL239.00 - NULL697.00
    Choose Options
  • Benazepril hydrochloride

    Biovision | Benazepril hydrochloride | B2138

    Benazepril is a prodrug of the angiotensin converting enzyme (ACE) inhibitor benazeprilat. It is metabolized to benazeprilat by hepatic esterases. Benazepril inhibits the in vitro enzymatic activity of partially purified ACE isolated from rabbit lung...

    NULL205.00 - NULL452.00
    Choose Options
  • 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 significantly reduces elevated LDL-C levels in patients...

    NULL271.00 - NULL828.00
    Choose Options
  • Belizatinib (TSR-011)

    Biovision | Belizatinib (TSR-011) | B2028

    Belizatinib (TSR-011) is a potent inhibitor of both the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) and the tropomyosin-related kinases (TRK) TRKA, TRKB, and TRKC, with potential antineoplastic activity. The inhibition leads to disruption...

    NULL320.00 - NULL1,024.00
    Choose Options
  • 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 7.5 and 9.5, respectively. It does not inhibit murine...

    NULL173.00 - NULL443.00
    Choose Options
  • 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 affect mitochondria by depleting the transmembrane...

    NULL222.00 - NULL616.00
    Choose Options
  • 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 function, converting it from a survival molecule to a...

    NULL303.00 - NULL967.00
    Choose Options
  • BD 1047 dihydrobromide

    Biovision | BD 1047 dihydrobromide | B1069

    BD1047 is a potent and selective Sigma-1 Receptor antagonist. BD-1047 has >50-fold selectivity at σ1 over σ2 and also >100-fold selectivity over opiate, phencyclidine, muscarinic, dopamine, α1- & α2-adrenoceptor, 5-HT1, and 5-HT2.BD1047 is a potent and...

    NULL271.00 - NULL828.00
    Choose Options
  • BCl-2 Inhibitor, ABT-199

    Biovision | BCl-2 Inhibitor, ABT-199 | 2253

    Cell-permeable. A potent and selective BCl-2 inhibitor that spares platelets while achieving potent antitumor activity.ABT-199 is a potent and selective BCl-2 inhibitor that spares platelets while achieving potent antitumor activity.Biovision | 2253 |...

    NULL231.00 - NULL476.00
    Choose Options
  • 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 selective RET and JAK2 inhibitor. It impairs GDNF-RET...

    NULL303.00 - NULL959.00
    Choose Options
  • 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 >100-fold selectivity over all other bromodomains...

    NULL288.00 - NULL861.00
    Choose Options
  • BAY-1895344 hydrochloride

    Biovision | BAY-1895344 hydrochloride | B1962

    BAY-1895344, an orally available, potent ATR (ataxia telangiectasia and Rad3-related) protein inhibitor (IC₅₀ = 7 nM). Displays potent anti-tumor efficacy in monotherapy and strong combination potential with the targeted alpha therapy Radium-223...

    NULL452.00 - NULL1,549.00
    Choose Options
  • 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 binds to and inhibits the activity of Mps1. This...

    NULL288.00 - NULL894.00
    Choose Options
  • 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 hypertensive effects.Molidustat (BAY-85-3934) is a novel...

    NULL303.00 - NULL959.00
    Choose Options
  • 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 phosphorylation by PI3Kα compared with PI3Kβ in cells. Shows...

    NULL369.00 - NULL1,222.00
    Choose Options
  • 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 Name/Synonyms: Methyl...

    NULL337.00 - NULL1,041.00
    Choose Options
  • Bay 61-3606 Hydrochloride

    Biovision | Bay 61-3606 Hydrochloride | 1796

    Cell-permeable. A potent, ATP-competitive and reversible inhibitor of spleen tyrosine kinase (Syk) (IC₅₀ = 10 nM). Displays excellent selectivity against many other kinases including Btk, Fyn, Itk, Lyn and Src up to concentrations of 4.7 µM. Shows good...

    NULL247.00 - NULL730.00
    Choose Options
  • BAY 58-2667 Hydrochloride

    Biovision | BAY 58-2667 Hydrochloride | 2027

    A nitric oxide (NO)- and heme-independent soluble guanylyl cyclase activator. Displays potent cardiovascular effects. Improves cardiopulmonary hemodynamics in patients with acute decompensated heart failure. Exhibits potent vasodilator and antiplatelet...

    NULL567.00 - NULL5,210.00
    Choose Options
  • BAY 58-2667 (Free base)

    Biovision | BAY 58-2667 (Free base) | 2452

    A free base form of the nitric oxide (NO)- and heme-independent soluble guanylyl cyclase activator BAY 58-2667 hydrochloride (Cat. No. 2027).BAY 58-2667 is a nitric oxide (NO)- and heme-independent soluble guanylyl cyclase activator. Displays potent...

    NULL541.00 - NULL1,713.00
    Choose Options
  • 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 viral primase-helicase complex. In various rodent...

    NULL239.00 - NULL3,200.00
    Choose Options
  • BAY 43-9006, Free base

    Biovision | BAY 43-9006, Free base | 2142

    A free base form of BAY 43-9006 (Sorafenib) (Cat. No. 1594-25,100). Acts as an inhibitor of Raf-1 and B-Raf (IC₅₀ = 6 and 22 nM, respectively), as well as several receptor tyrosine kinases, including VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit (IC₅₀ = 90,...

    NULL263.00 - NULL639.00
    Choose Options
  • BAY 43-9006 (Tosylate)

    Biovision | BAY 43-9006 (Tosylate) | 1594

    BAY 43-9006 (Sorafenib) is an inhibitor of Raf-1 and B-Raf (IC₅₀ = 6 and 22 nM, respectively), as well as several receptor tyrosine kinases, including VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit (IC₅₀ = 90, 15, 20, 57, and 58 nM, respectively. It poorly...

    NULL280.00 - NULL656.00
    Choose Options
  • 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 oligomerization, BAX-mediated pore formation and...

    NULL239.00 - NULL697.00
    Choose Options
  • Batimastat (MMP Inhibitor)

    Biovision | Batimastat (MMP Inhibitor) | 1704

    Potent, broad spectrum matrix metalloprotease (MMP) inhibitor (IC₅₀ values are 3, 4, 4, 6 and 20 nM for MMP -1, -2, -9, -7 and -3 respectively). Exhibits antiproliferative, anti-invasive and antimetastatic activity in human ovarian carcinoma xenografts...

    NULL280.00 - NULL639.00
    Choose Options
  • Baricitinib phosphate

    Biovision | Baricitinib phosphate | 2841

    Baricitinib phosphate is a selective JAK1 and JAK2 inhibitor with IC₅₀ values of 5.9 nM and 5.7 nM, respectively. Baricitinib is ~70 and ~10-fold selective versus JAK3 and Tyk2, with no inhibition to c-Met and Chk2.Baricitinib phosphate is a selective...

    NULL271.00 - NULL828.00
    Choose Options
  • 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 fibrosis. BAR502 protects against liver damage caused by...

    NULL303.00 - NULL959.00
    Choose Options
  • 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 of GLUTAg cells to BAR501 (10 μM) increases the...

    NULL303.00 - NULL959.00
    Choose Options
  • 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 cell-permeable, selective chelator of intracellular...

    NULL173.00 - NULL403.00
    Choose Options
  • 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.BAG 956 is a potent, ATP-competitive, dual PI3K/PDK-1...

    NULL288.00 - NULL861.00
    Choose Options
  • 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 study disruption of bacterial cell wall synthesis at the...

    NULL239.00 - NULL656.00
    Choose Options
  • 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 μM). Displays 100-fold selectivity for HIV reverse...

    NULL190.00 - NULL452.00
    Choose Options
  • 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 harboring sensitizing EGFR mutants with mean IC₅₀ values...

    NULL205.00 - NULL567.00
    Choose Options