Non-Antibody Products — page 1 of 22,244



Non-Antibody Products
Page 1 of 22,244
  • Records 1 - 100 of 2,224,306
Name Description Size Catalog # Supplier
A-366 Purity ≥98% by HPLC. Background: A-366 is a potent and selective G9a /… 1 mg, 5 mg MBS842453 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-366 Purity ≥98%. MW: 329.444 100 mg, 500 mg MBS131198 MYBIOSOURCE INC.
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.
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.
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.
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.
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.
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.
MYBIOSOURCE INC.
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A66 MW: 393.53 10 mg MBS8506193 MYBIOSOURCE INC.
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.
MYBIOSOURCE INC.
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A66 Purity 97%+. MW: 393.53 2 mg, 5 mg, 1ml/10mM (in DMSO) MBS575616 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-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.
MYBIOSOURCE INC.
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A-674563 Purity ≥98%. MW: 358.445 100 mg, 500 mg MBS131746 MYBIOSOURCE INC.
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.
MYBIOSOURCE INC.
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A-769662 Purity ≥98% by HPLC. Background: Cell-permeable. A potent AMPK activato… 5 mg MBS842018 MYBIOSOURCE INC.
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.
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.
MYBIOSOURCE INC.
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A77-01 Purity ≥98%. MW: 286.33 2 mg, 5 mg, 1ml/10mM (in DMSO) MBS577536 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77-01 Purity ≥98%. MW: 286.338 100 mg, 500 mg MBS130865 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98% (TLC). MW: 357.8 10 mg, 50 mg MBS565381 MYBIOSOURCE INC.
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.
MYBIOSOURCE INC.
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A-803467 Purity ≥98%. MW: 357.79 100 mg, 500 mg MBS132100 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98%. MW: 357.79 1ml/10mM (in DMSO), 10 mg, 25 mg MBS575739 MYBIOSOURCE INC.
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.
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.
MYBIOSOURCE INC.
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A-83-01 Purity 97%+. MW: 421.52 2 mg, 5 mg, 10 mg MBS575483 MYBIOSOURCE INC.
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.
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.
MYBIOSOURCE INC.
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A-966492 Purity ≥98%. MW: 324.359 100 mg, 500 mg MBS132689 MYBIOSOURCE INC.
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.
MYBIOSOURCE INC.
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A1120 n/a n/a A3111 MILLIPORE-SIGMA
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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A-740003 A-740003 is a potent and selective competitive antagonist of P2X7 receptor… 50 mg A-420 ALOMONE LABS
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A-794278 A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… 10 mg A-435 ALOMONE LABS
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A-794278 A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… 25 mg A-435 ALOMONE LABS
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A-794278 A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… 5 mg A-435 ALOMONE LABS
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A-794278 A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… 50 mg A-435 ALOMONE LABS
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A-803467 A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… 10 mg A-105 ALOMONE LABS
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A-803467 A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… 100 mg A-105 ALOMONE LABS
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A-803467 A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… 25 mg A-105 ALOMONE LABS
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A-803467 A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… 50 mg A-105 ALOMONE LABS
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A-804598 A-804598 is a potent and selective, competitive and high-affinity antagoni… 10 mg A-415 ALOMONE LABS
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A-804598 A-804598 is a potent and selective, competitive and high-affinity antagoni… 25 mg A-415 ALOMONE LABS
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A-804598 A-804598 is a potent and selective, competitive and high-affinity antagoni… 5 mg A-415 ALOMONE LABS
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A-804598 A-804598 is a potent and selective, competitive and high-affinity antagoni… 50 mg A-415 ALOMONE LABS
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A-839977 A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… 10 mg A-470 ALOMONE LABS
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A-839977 A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… 25 mg A-470 ALOMONE LABS
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A-839977 A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… 5 mg A-470 ALOMONE LABS
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A-839977 A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… 50 mg A-470 ALOMONE LABS
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A-841720 A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… 10 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… 25 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… 5 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… 50 mg A-440 ALOMONE LABS
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A-850002 A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… 10 mg A-390 ALOMONE LABS
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A-850002 A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… 25 mg A-390 ALOMONE LABS
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A-850002 A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… 5 mg A-390 ALOMONE LABS
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A-850002 A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… 50 mg A-390 ALOMONE LABS
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A-889425 A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… 1 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… 10 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… 25 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… 5 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… 50 mg A-195 ALOMONE LABS
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293A The HEK 293A cell line is an immortalized line of primary human embryonic… 1 vial ABI-TC1333 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A10.7 Derived from metastatic liver tumor (clinical stage IV). 1 vial ABC-TC533S ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A-172 Organ: brain Disease: glioblastoma. 1 vial ABC-TC0022 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A-204 Human Muscle Rhabdomyosarcoma cell line. The A-204 cell line was establish… 1 vial ABC-TC445S ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A2058 Malignant melanoma, metastasis to lymph node. 1 vial ABC-TC0023 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A-253 The A253 line is one of thirteen to be isolated and partially characterize… 1 vial ABC-TC0024 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A375 This line was derived from a 54 year old female with malignant melanoma. 1 vial ABC-TC0026 ACCEGEN BIOTECH
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A-427 A-427 cell line was established from the lung carcinoma of a 52-year-old C… 1 vial ABC-TC1339 ACCEGEN BIOTECH
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A-431 The epidermoid carcinoma cell line A-431, derived from an 85-year-old fema… 1 vial ABC-TC0030 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A-498 Established from the kidney carcinoma of a 52-year-old man in 1973. 1 vial ABC-TC0031 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A549 A549 cell line was initiated in 1972 by D.J. Giard, et al. Through explant… 1 vial ABC-TC0032 ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A6 Frog (Xenopus laevis) cell line derived from kidney. Lifespan: infinite. 1 vial ABC-TC020S ACCEGEN BIOTECH
ACCEGEN BIOTECH
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A-673 Tissue: muscle Disease: rhabdomyosarcoma. 1 vial ABC-TC0034 ACCEGEN BIOTECH
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A-704 Human kidney adenocarcinoma. Derived from 78-year-old male. Does not produ… 1 vial ABC-TC0021 ACCEGEN BIOTECH
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A-72 Canine Golden Retriever tumour. Derived from tumour of thigh (unknown hist… 1 vial ABC-TC0036 ACCEGEN BIOTECH
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A9 Mouse C3H / An areolar and adipose tissue. Derivative of L929 selected in… 1 vial ABC-TC0037 ACCEGEN BIOTECH
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