Non-Antibody Products — page 1 of 29,398



Non-Antibody Products
Page 1 of 29,398
  • Records 1 - 50 of 1,469,890
Name Description Size Catalog # Supplier
293 n/a n/a 103 NIH AIDS REAGENT PROGRAM
NIH AIDS REAGENT PROGRAM
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968 n/a 10mg, 50mg 254461 UNITED STATES BIOLOGICAL
UNITED STATES BIOLOGICAL
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968 Allosteric inhibitor of glutaminase. Blocks Rho-GTPase-dependent transform… 10 mg 5460/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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968 Allosteric inhibitor of glutaminase. Blocks Rho-GTPase-dependent transform… 50 mg 5460/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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6877002 CD40-TRAF6 interaction inhibitor. Suppresses CD40-induced IL-1β and I… 10 mg 5602/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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6877002 CD40-TRAF6 interaction inhibitor. Suppresses CD40-induced IL-1β and I… 50 mg 5602/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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666-15 Potent and selective CREB inhibitor (IC50 = 81 nM). Inhibits cancer cell g… 10 mg 5661/10 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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666-15 Potent and selective CREB inhibitor (IC50 = 81 nM). Inhibits cancer cell g… 50 mg 5661/50 TOCRIS BIOSCIENCE
TOCRIS BIOSCIENCE
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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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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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571188-59-5 571188-59-5 is a chemical reagent. 5 g, 25 g, 100 g abx185252 ABBEXA
ABBEXA
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A3.01 n/a n/a 166 NIH AIDS REAGENT PROGRAM
NIH AIDS REAGENT PROGRAM
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A2.01 n/a n/a 2059 NIH AIDS REAGENT PROGRAM
NIH AIDS REAGENT PROGRAM
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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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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-769662 MW: 360.39. Purity ≥98% by HPLC. Background: Cell-permeable. A potent A… 5 mg MBS842018 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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A-803467 MW: 357.8. Purity ≥98% by TLC. Background: A-803467 is a potent, select… 5 mg, 25 mg MBS842200 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-887826 MW: 480.99. A structurally novel, potent and voltage-dependent Nav1.8 sodi… 10 mg MBS6025868 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 922500 MW: 428.48. 5 mg MBS8506458 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 MW: 358.44. 2 mg MBS8506244 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-779 MW: 872.99. Purity >95% 1 mg, 5 mg, 10 mg MBS826669 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 1 mg 9001799-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 10 mg 9001799-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 25 mg 9001799-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 5 mg 9001799-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 1 mg 18317-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 10 mg 18317-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 5 mg 18317-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 500 µg 18317-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 1 mg 11016-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 10 mg 11016-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 25 mg 11016-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 5 mg 11016-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 10 mg 16081-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 5 mg 16081-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 50 mg 16081-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 1 mg 16499-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 5 mg 16499-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 500 µg 16499-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 1 mg 17358-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 10 mg 17358-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 5 mg 17358-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 1 mg 17382-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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