Non-Antibody Products — page 14,269 of 21,993
Non-Antibody Products
Page 14,269 of 21,993
| Name | Description | Size | Catalog # | Supplier | |
|---|---|---|---|---|---|
| 88255-01-0 | Purity ≥98%. MW: 420.46 | 100 mg, 500 mg | MBS132338 |
 MYBIOSOURCE INC. |
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| 95343-20-7 | Purity ≥98%. MW: 664.1 | 100 mg, 500 mg | MBS130215 |
MYBIOSOURCE INC. |
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| 92.1 | Tissue: uvea; Tumor: melanoma, melanin production. | 1 vial | ABC-TC444S |
 ACCEGEN BIOTECH |
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| 380 | Tissue: peripheral blood; Tumor: leukemia, pre-B cell; Derived from a pati… | 1 vial | ABC-TC442S |
ACCEGEN BIOTECH |
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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 |
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| 5637 | 5637 Cell line was established from the primary bladder carcinoma of a 68-… | 1 vial | ABC-TC0015 |
ACCEGEN BIOTECH |
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| 666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 10 mg | 30780-10 |
 CAYMAN CHEMICAL COMPANY |
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| 666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 25 mg | 30780-25 |
CAYMAN CHEMICAL COMPANY |
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| 666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 5 mg | 30780-5 |
CAYMAN CHEMICAL COMPANY |
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| 666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 50 mg | 30780-50 |
CAYMAN CHEMICAL COMPANY |
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| 13323-67-6 | Purity ≥98%. MW: 286.3 | 5 mg | orb1290280 |
 BIORBYT LTD. |
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| 1360900-71-5 | MW: 228.0427 | 100 mg | orb1146568 |
BIORBYT LTD. |
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| 14787-34-9 | Purity ≥98%. MW: 358.4 | 5 mg | orb1290300 |
BIORBYT LTD. |
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| 1776-30-3 | Purity ≥98%. MW: 240.3 | 20 mg | orb1290287 |
BIORBYT LTD. |
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| 20127-63-3 | Purity ≥98%. MW: 196.2 | 20 mg | orb1290297 |
BIORBYT LTD. |
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| 408324-00-5 | Purity ≥98%. MW: 332.4 | 5 mg | orb1290294 |
BIORBYT LTD. |
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| 42206-91-7 | Purity ≥98%. MW: 372.4 | 10 mg | orb1290298 |
BIORBYT LTD. |
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| 53596-71-7 | Purity ≥98%. MW: 242.3 | 20 mg | orb1290277 |
BIORBYT LTD. |
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| 653-47 | Purity 98.00%. MW: 370.83 | 50 mg, 100 mg | orb1685345 |
BIORBYT LTD. |
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| 666-15 | 666-15 is a potent and selective CREB inhibitor with an IC50 of 81 nM. MW:… | 1 g, 100 mg, 250 mg, 10 mM * 1 mL in DMSO | orb401883 |
BIORBYT LTD. |
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| 666-15 | Purity 99.77%. MW: 620.52 | 200 mg, 100 mg, 1 mg, 50 mg, 25 mg, 10 mg, 5 mg | orb1301894 |
BIORBYT LTD. |
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| 666-15 | n/a | 5 mg, 10 mg, 50 mg | orb1889352 |
BIORBYT LTD. |
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| 8011-6561 | Purity 98.00%. MW: 291.39 | 5 mg, 50 mg, 100 mg | orb1709067 |
BIORBYT LTD. |
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| 8- | MW: 232.191 | 5 mg | orb421163 |
BIORBYT LTD. |
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| 293 | n/a | n/a | 103 |
 NIH AIDS REAGENT PROGRAM |
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| A 205804 | Purity ≥98%. MW: 300.39 | 100 mg, 500 mg | MBS132392 |
MYBIOSOURCE INC. |
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| A 66 | Purity ≥98%. MW: 393.52 | 100 mg, 500 mg | MBS132169 |
MYBIOSOURCE INC. |
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| A 740003 | Purity ≥98%. MW: 474.565 | 100 mg, 500 mg | MBS132187 |
MYBIOSOURCE INC. |
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| A 740003 | Purity >98%. A 740003 is a novel competitive antagonist of P2X7 receptors… | 10 mg, 25 mg, 50 mg | MBS384091 |
MYBIOSOURCE INC. |
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| A 769662 | Purity ≥98%. MW: 360.39 | 100 mg, 500 mg | MBS130892 |
MYBIOSOURCE INC. |
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| A 769662 | Purity 97%+. MW: 360.39 | 5 mg, 1ml/10mM (in DMSO), 10 mg | MBS576261 |
MYBIOSOURCE INC. |
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| A 803467 | Purity >98%. A 803467 is a selective blocker of NaV1.8 channels (IC50 valu… | 10 mg, 1 mL (in DMSO), 25 mg | MBS384093 |
MYBIOSOURCE INC. |
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| A 83-01 | Purity ≥98% by HPLC. Background: A selective inhibitor of TGF-beta type… | 1 mg | MBS842636 |
MYBIOSOURCE INC. |
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| A 83-01 | Purity ≥98%. MW: 421.52 | 100 mg, 500 mg | MBS132328 |
MYBIOSOURCE INC. |
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| A 83-01 | Purity >98%. A83-01 is a TGF-β kinase / activin receptor like kinase… | 5 mg, 10 mg, 25 mg | MBS384095 |
MYBIOSOURCE INC. |
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| A 922500 | MW: 428.48 | 5 mg | MBS8506458 |
MYBIOSOURCE INC. |
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| A 922500 | Purity ≥98%. MW: 428.488 | 100 mg, 500 mg | MBS130245 |
MYBIOSOURCE INC. |
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| A 967079 | Purity >98%. A 967079 is a selective TRPA1 channel blocker (IC50 values ar… | 10 mg, 25 mg, 50 mg | MBS384097 |
MYBIOSOURCE INC. |
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| A-1155463 | Purity >98%. A-1155463 is a highly potent and selective BCL-XL inhibitor,… | 5 mg, 10 mg, 50 mg | MBS384082 |
MYBIOSOURCE INC. |
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| A-1210477 | Purity ≥98%. MW: 886.51 | 100 mg, 500 mg | MBS131280 |
MYBIOSOURCE INC. |
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| A-1210477 | Purity ≥99%. MW: 850.04 | 2 mg, 5 mg, 10 mg | MBS575263 |
MYBIOSOURCE INC. |
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| A-1210477 | Purity >98%. A-1210477 is a potent and selective MCL-1 inhibitor. A-121047… | 5 mg, 10 mg, 25 mg | MBS384084 |
MYBIOSOURCE INC. |
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| A-1331852 | Purity ≥98%. MW: 658.82 | 100 mg, 500 mg | MBS131656 |
MYBIOSOURCE INC. |
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| A-196 | Purity ≥99%. A-196 is a potent and selective inhibitor of SUV420 h1 and… | 2 mg, 1ml/10mM (in DMSO), 5 mg | MBS5750478 |
MYBIOSOURCE INC. |
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| A-205804 | Purity 97%+. MW: 300.41 | 5 mg, 10 mg, 1ml/10mM (in DMSO) | MBS576130 |
MYBIOSOURCE INC. |
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| A23187 | Purity >98% by TLC. Background: A calcium ionophore. Causes rapid influx o… | 10 mg | MBS843148 |
MYBIOSOURCE INC. |
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| A-366 | Purity ≥98% by HPLC. Background: A-366 is a potent and selective G9a /… | 1 mg, 5 mg | MBS842453 |
MYBIOSOURCE INC. |
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| A-366 | Purity ≥98%. MW: 329.444 | 100 mg, 500 mg | MBS131198 |
MYBIOSOURCE INC. |
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| A-366 | Purity >98%. A-366 is a potent and selective G9a / GLP histone lysine meth… | 10 mg, 25 mg, 50 mg | MBS384085 |
MYBIOSOURCE INC. |
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| A427 | A427 cells are derived from human lung epithelial carcinoma taken from a 5… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201043 |
MYBIOSOURCE INC. |
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| A431 | A431 cells were established from an epidermoid carcinoma in the skin / epi… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201022 |
MYBIOSOURCE INC. |
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| A-443654 | Purity >98%. A-443654, a specific Akt inhibitor with Ki value of 160 pM, i… | 2 mg, 5 mg, 10 mg | MBS384086 |
MYBIOSOURCE INC. |
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| A-484954 | Purity >98%. A-484954 is a potent, selective inhibitor of eukaryotic longa… | 10 mg, 25 mg, 50 mg | MBS384087 |
MYBIOSOURCE INC. |
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| A549 | A549 cells are adenocarcinomic human alveolar basal epithelial cells. The… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201023 |
MYBIOSOURCE INC. |
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| A66 | MW: 393.53 | 10 mg | MBS8506193 |
MYBIOSOURCE INC. |
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| A66 | Purity >98%. The S-enantiomer of A66 is a potent inhibitor of the p110alph… | 5 mg, 1 mL (in DMSO), 10 mg | MBS384089 |
MYBIOSOURCE INC. |
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| A66 | Purity 97%+. MW: 393.53 | 2 mg, 5 mg, 1ml/10mM (in DMSO) | MBS575616 |
MYBIOSOURCE INC. |
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| A-674563 | MW: 358.44 | 2 mg | MBS8506244 |
MYBIOSOURCE INC. |
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| A-674563 | Purity ≥98%. A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest pot… | 1 mg, 2 mg, 5 mg | MBS578707 |
MYBIOSOURCE INC. |
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| A-674563 | Purity ≥98%. MW: 358.445 | 100 mg, 500 mg | MBS131746 |
MYBIOSOURCE INC. |
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| A-674563 | Purity >98%. A-674563 is a B / Akt inhibitor with an IC50 of 14 nM and als… | 5 mg, 1 mL (in DMSO), 10 mg | MBS384090 |
MYBIOSOURCE INC. |
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| A-769662 | Purity ≥98% by HPLC. Background: Cell-permeable. A potent AMPK activato… | 5 mg | MBS842018 |
MYBIOSOURCE INC. |
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| A-769662 | Purity >98%. A-769662 is a new activator of AMP-activated protein kinase (… | 5 mg, 10 mg, 1 mL (in DMSO) | MBS384092 |
MYBIOSOURCE INC. |
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| A77 1726 | Purity ≥98% by HPLC. Background: Physiologically active metabolite of t… | 5 mg, 25 mg | MBS842963 |
MYBIOSOURCE INC. |
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| A77-01 | Purity ≥98%. MW: 286.33 | 2 mg, 5 mg, 1ml/10mM (in DMSO) | MBS577536 |
MYBIOSOURCE INC. |
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| A77-01 | Purity ≥98%. MW: 286.338 | 100 mg, 500 mg | MBS130865 |
MYBIOSOURCE INC. |
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| A-803467 | Purity ≥98% (TLC). MW: 357.8 | 10 mg, 50 mg | MBS565381 |
MYBIOSOURCE INC. |
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| A-803467 | Purity ≥98% by TLC. Background: A-803467 is a potent, selective inhibit… | 5 mg, 25 mg | MBS842200 |
MYBIOSOURCE INC. |
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| A-803467 | Purity ≥98%. MW: 357.79 | 100 mg, 500 mg | MBS132100 |
MYBIOSOURCE INC. |
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| A-803467 | Purity ≥98%. MW: 357.79 | 1ml/10mM (in DMSO), 10 mg, 25 mg | MBS575739 |
MYBIOSOURCE INC. |
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| A-804598 | Purity >98%. A-804598 is a P2X7 selective, competitive antagonist with the… | 5 mg, 10 mg, 25 mg | MBS384094 |
MYBIOSOURCE INC. |
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| A83-01 | Purity >98% (TLC); NMR (Conforms). ALK inhibitor. Selective glycogen synth… | 5 mg, 25 mg | MBS515040 |
MYBIOSOURCE INC. |
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| A-83-01 | Purity 97%+. MW: 421.52 | 2 mg, 5 mg, 10 mg | MBS575483 |
MYBIOSOURCE INC. |
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| A-966492 | A-966492 is a highly potent and efficacious poly(ADP-ribose) polymerase (P… | 10 mg | MBS8506196 |
MYBIOSOURCE INC. |
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| A-966492 | Purity ≥98%. A-966492 is a novel and potent inhibitor of PARP1 and PARP… | 2 mg, 5 mg, 1ml/10mM (in DMSO) | MBS578914 |
MYBIOSOURCE INC. |
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| A-966492 | Purity ≥98%. MW: 324.359 | 100 mg, 500 mg | MBS132689 |
MYBIOSOURCE INC. |
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| A-966492 | Purity >98%. A-966492 displayed high potency against the poly(ADP-ribose)… | 5 mg, 1 mL (in DMSO), 10 mg | MBS384096 |
MYBIOSOURCE INC. |
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| A1120 | n/a | n/a | A3111 |
 MILLIPORE-SIGMA |
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| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 10 mg | A-345 |
 ALOMONE LABS |
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| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 25 mg | A-345 |
ALOMONE LABS |
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| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 5 mg | A-345 |
ALOMONE LABS |
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| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 50 mg | A-345 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 10 mg | A-225 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 100 mg | A-225 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 25 mg | A-225 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 250 mg | A-225 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 5 mg | A-225 |
ALOMONE LABS |
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| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 50 mg | A-225 |
ALOMONE LABS |
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| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 1 mg | A-360 |
ALOMONE LABS |
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| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 10 mg | A-360 |
ALOMONE LABS |
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| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 25 mg | A-360 |
ALOMONE LABS |
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| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 5 mg | A-360 |
ALOMONE LABS |
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| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 1 mg | A-600 |
ALOMONE LABS |
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| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 mg | A-600 |
ALOMONE LABS |
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| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 x 1 mg | A-600 |
ALOMONE LABS |
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| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 mg | A-600 |
ALOMONE LABS |
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| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 x 5 mg | A-600 |
ALOMONE LABS |
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| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 10 mg | A-420 |
ALOMONE LABS |
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| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 100 mg | A-420 |
ALOMONE LABS |
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| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 25 mg | A-420 |
ALOMONE LABS |
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