Non-Antibody Products — page 1 of 15,005



Non-Antibody Products
Page 1 of 15,005
  • Records 1 - 100 of 1,500,466
Name Description Size Catalog # Supplier
968 n/a 10mg, 50mg 254461 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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666-15 MW: 620.52. Purity >98% 100 mg, 250 mg, 1 g orb401883 BIORBYT LTD.
BIORBYT LTD.
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968 Purity 99%. MW (observed): 475.42. Allosteric inhibitor of glutaminase. Bl… 10 mg 5460/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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968 Purity 99%. MW (observed): 475.42. Allosteric inhibitor of glutaminase. Bl… 50 mg 5460/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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6877002 Purity 99%. MW (observed): 251.32. CD40-TRAF6 interaction inhibitor. Suppr… 10 mg 5602/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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6877002 Purity 99%. MW (observed): 251.32. CD40-TRAF6 interaction inhibitor. Suppr… 50 mg 5602/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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666-15 Purity 98%. MW (observed): 620.52. Potent and selective CREB inhibitor (IC… 10 mg 5661/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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666-15 Purity 98%. MW (observed): 620.52. Potent and selective CREB inhibitor (IC… 50 mg 5661/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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571188-59-5 571188-59-5 is a chemical reagent. 5 g, 25 g, 100 g abx185252 ABBEXA
ABBEXA
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293 n/a n/a 103 NIH AIDS REAGENT PROGRAM
NIH AIDS REAGENT PROGRAM
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1301 Human T-cell leukaemia. 1301 is a sub-line of CCRF-CEM. It has unusually l… 1 vial ABC-TC0001 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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5637 5637 cell line was established from the primary bladder carcinoma of a 68-… 1 vial ABC-TC0015 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A 83-01 A selective inhibitor of TGF-β type I receptor ALK5 kinase, type I ac… 1 mg 1725-1 BIOVISION, INC.
BIOVISION, INC.
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A-1155463 A-1155463 is a highly potent and selective BCL-XL inhibitor. A-1155463 is… 5 mg B1821-5 BIOVISION, INC.
BIOVISION, INC.
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A-1155463 A-1155463 is a highly potent and selective BCL-XL inhibitor. A-1155463 is… 25 mg B1821-25 BIOVISION, INC.
BIOVISION, INC.
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A-1210477 A-1210477 is a potent MCL-1 inhibitor (Ki = 0.45 nM in TR-FRET-binding ass… 5 mg B1826-5 BIOVISION, INC.
BIOVISION, INC.
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A-1210477 A-1210477 is a potent MCL-1 inhibitor (Ki = 0.45 nM in TR-FRET-binding ass… 25 mg B1826-25 BIOVISION, INC.
BIOVISION, INC.
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A-1331852 A-1331852 is a potent anti-apoptotic Bcl-xL protein inhibitor and apoptosi… 5 mg B1948-5 BIOVISION, INC.
BIOVISION, INC.
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A-1331852 A-1331852 is a potent anti-apoptotic Bcl-xL protein inhibitor and apoptosi… 25 mg B1948-25 BIOVISION, INC.
BIOVISION, INC.
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A23187 A calcium ionophore. Causes rapid influx of calcium in various cells. MW:… 10 mg 1501-10 BIOVISION, INC.
BIOVISION, INC.
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A-366 A-366 is a potent and selective G9a / GLP histone lysine methyltransferase… 1 mg 2859-1 BIOVISION, INC.
BIOVISION, INC.
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A-366 A-366 is a potent and selective G9a / GLP histone lysine methyltransferase… 5 mg 2859-5 BIOVISION, INC.
BIOVISION, INC.
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A37 A37 is a aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitor (IC50 = 4.6 µ… 5 mg B1577-5 BIOVISION, INC.
BIOVISION, INC.
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A37 A37 is a aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitor (IC50 = 4.6 µ… 25 mg B1577-25 BIOVISION, INC.
BIOVISION, INC.
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A66 A66 is a highly specific and selective p110α inhibitor with IC50 of… 5 mg B1654-5 BIOVISION, INC.
BIOVISION, INC.
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A66 A66 is a highly specific and selective p110α inhibitor with IC50 of… 25 mg B1654-25 BIOVISION, INC.
BIOVISION, INC.
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A-769662 Cell-permeable. A potent AMPK activator. Directly stimulates partially pur… 5 mg 1719-5 BIOVISION, INC.
BIOVISION, INC.
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A77 1726 Physiologically active metabolite of the immunosuppressive drug leflunomid… 5 mg 1973-5 BIOVISION, INC.
BIOVISION, INC.
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A77 1726 Physiologically active metabolite of the immunosuppressive drug leflunomid… 25 mg 1973-25 BIOVISION, INC.
BIOVISION, INC.
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A-803467 A-803467 is a potent, selective inhibitor of the TTX-resistant voltage-gat… 5 mg 2559-5 BIOVISION, INC.
BIOVISION, INC.
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A-803467 A-803467 is a potent, selective inhibitor of the TTX-resistant voltage-gat… 25 mg 2559-25 BIOVISION, INC.
BIOVISION, INC.
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A 1070722 n/a 10mg, 50mg 254462 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 1120 n/a 10mg, 50mg 254463 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 205804 n/a 10mg, 50mg 254464 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 286982 n/a 10mg, 50mg 254465 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 438079 Purity ~99% (HPLC). A potent, competitive, and selective antagonist of P2X… 10mg 217134 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 484954 n/a 10mg, 50mg 254471 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 582941 n/a 10mg, 50mg 254472 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 740003 n/a 10mg, 50mg 254475 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 769662 n/a 10mg, 50mg 254476 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 784168 n/a 10mg, 50mg 254478 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 803467 n/a 10mg, 50mg 254479 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 804598 n/a 10mg, 50mg 254481 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 83-01 n/a 10mg 162480 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 83-01 n/a 10mg, 50mg 254482 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 839977 n/a 10mg, 50mg 254483 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 841720 n/a 10mg, 50mg 254484 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 844606 n/a 10mg, 50mg 254485 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 867744 n/a 10mg, 50mg 254487 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 887826 n/a 10mg, 50mg 254488 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 922500 n/a 10mg 254489 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 967079 n/a 10mg, 50mg 254491 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A 987306 n/a 10mg, 50mg 254492 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A01 n/a 10mg, 50mg 254495 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A1803 n/a 5mg, 10mg, 25mg 258663 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A317491 Purity ~99% (HPLC). A potent, selective, and competitive non-nucleotide an… 5mg 217136 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A-674563 Highly Purified (~95%). Three related forms of the kinase Akt (1, 2, 3, al… 500ug, 1mg, 5mg 349624 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A-71623 n/a 1mg 254494 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A-887826 A structurally novel, potent and voltage-dependent Nav1.8 sodium channel b… 10mg 1003 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A-887826 n/a 5mg, 10mg, 25mg 258686 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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A-1155463 Ki=19 nM A-1155463 is a potent and selective BCL-XL inhibitor. BCL-2 plays… multiple CC326 CROWN BIOSCIENCE INC.
CROWN BIOSCIENCE INC.
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A-1210477 A-1210477 is an effective and specific MCL-1 inhibitor with an EC50 value… multiple CC323 CROWN BIOSCIENCE INC.
CROWN BIOSCIENCE INC.
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A-443654 A-443654 is a potent and selective inhibitor of Akt with Ki value of 160 p… multiple CC349 CROWN BIOSCIENCE INC.
CROWN BIOSCIENCE INC.
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A66 A66 is a potent and selective p110a inhibitor with IC50 of 32 nM. P110a is… multiple CC389 CROWN BIOSCIENCE INC.
CROWN BIOSCIENCE INC.
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A-674563 A-674563 is a potent and selective Akt1 inhibitor with IC50 value of 14 nM… multiple CC399 CROWN BIOSCIENCE INC.
CROWN BIOSCIENCE INC.
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A83-01 ALK inhibitor. MW: 421.5 Da. Purity >98% (TLC); NMR (Conforms) 5 mg A09-900-05 SIGNALCHEM
SIGNALCHEM
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A83-01 ALK inhibitor. MW: 421.5 Da. Purity >98% (TLC); NMR (Conforms) 25 mg A09-900-25 SIGNALCHEM
SIGNALCHEM
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A-674563 MW: 358.44, Purity >98% . A-674563 is a potent, orally available Akt1 inhi… 5 mg B1761-5 BIOVISION, INC.
BIOVISION, INC.
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A-674563 MW: 358.44, Purity >98% . A-674563 is a potent, orally available Akt1 inhi… 25 mg B1761-25 BIOVISION, INC.
BIOVISION, INC.
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A 740003 Purity 98%. Potent and selective P2X7 receptor antagonist (IC50 values are… 10 mg, 1ml/10mM (In DMSO), 50 mg, 100 mg MBS578551 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 769662 MW: 360.39. Purity 97%+ 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS576261 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 MW: 421.52. Purity ≥98% by HPLC. Background: A selective inhibitor of T… 1 mg MBS842636 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 922500 MW: 428.48. 5 mg MBS8506458 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1155463 Purity 98%. A-1155463, a highly potent and selective BCL-XL inhibitor, sho… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS579281 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1210477 MW: 850.04. Purity 99% 5 mg, 10 mg, 25 mg, 50 mg, 100 mg MBS575263 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1331852 Purity 98%. A-1331852 is a potent and selectiveBCL-XL inhibitor and may be… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS579282 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-205804 MW: 300.41. Purity 97%+ 2 mg, 5 mg, 10 mg, 1ml/10mM (In DMSO), 25 mg MBS576130 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A23187 MW: 523.6. Purity >98% by TLC. Background: A calcium ionophore. Causes rap… 10 mg MBS843148 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-366 MW: 329.44. Purity ≥98% by HPLC. Background: A-366 is a potent and sele… 1 mg, 5 mg MBS842453 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-366 Purity 98%. Potent and selective G9a / GLP histone lysine methyltransferas… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS578491 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A66 MW: 393.53. Purity 97%+ 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS575616 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A66 MW: 393.53. 10 mg MBS8506193 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-674563 Purity 98%. A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent… 2 mg, 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg MBS578707 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-674563 MW: 358.44. 2 mg MBS8506244 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77 1726 MW: 270.21. Purity ≥98% by HPLC. Background: Physiologically active met… 5 mg, 25 mg MBS842963 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77-01 MW: 286.33. Purity 98% 2 mg, 5 mg, 1ml/10mM (In DMSO), 10 mg MBS577536 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 MW: 357.79. Purity 98% 10 mg, 1ml/10mM (In DMSO), 25 mg, 50 mg MBS575739 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 MW: 357.8. Purity ≥98% (TLC) 10 mg, 50 mg MBS565381 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-804598 Purity 98%. A-804598 is a novel, competitive, and selective P2X7 receptor… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS578506 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A83-01 MW: 421.5. Purity >98% (TLC); NMR (Conforms). ALK inhibitorSelective glyco… 5 mg, 25 mg MBS515040 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-83-01 MW: 421.52. Purity 97%+ 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS575483 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 MW: 324.35. 10 mg MBS8506196 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 Purity 98%. A-966492 is a novel and potent inhibitor of PARP1 and PARP2 wi… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS578914 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 Purity >98% by HPLC. n/a LS-H2425 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A-1155463 Purity >98% by HPLC. n/a LS-H4227 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A-1210477 Purity >98% by HPLC. n/a LS-H4232 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A23187 Purity >98% by TLC. n/a LS-H2266 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A-366 Purity >98% by HPLC. n/a LS-H3403 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A37 Purity >98% by HPLC. n/a LS-H4115 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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A66 Purity >98%. n/a LS-H4188 LIFESPAN BIOSCIENCES INC.
LIFESPAN BIOSCIENCES INC.
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