Non-Antibody Products — page 23,552 of 44,716



Non-Antibody Products
Page 23,552 of 44,716
  • Records 1,177,551 - 1,177,600 of 2,235,767
Name Description Size Catalog # Supplier
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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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
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A6 Frog (Xenopus laevis) cell line derived from kidney. Lifespan: infinite. 1 vial ABC-TC020S ACCEGEN BIOTECH
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A-673 Tissue: muscle Disease: rhabdomyosarcoma. 1 vial ABC-TC0034 ACCEGEN BIOTECH
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
ACCEGEN BIOTECH
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10074-A4 An inhibitor of the protein-protein interaction between c-Myc and Max; inh… 1 mg 37486-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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10074-A4 An inhibitor of the protein-protein interaction between c-Myc and Max; inh… 10 mg 37486-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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10074-A4 An inhibitor of the protein-protein interaction between c-Myc and Max; inh… 25 mg 37486-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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10074-A4 An inhibitor of the protein-protein interaction between c-Myc and Max; inh… 5 mg 37486-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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