CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 752 of 1

Non-Antibody Products
Page 752 of 1,288
  • Records 37,551 - 37,600 of 64,374
Name Description Size Catalog #
MHAPC-Chol A cationic cholesterol; induces gene silencing in MCF-7 cells without affe… 10 mg 26585-10 More Info
MHAPC-Chol A cationic cholesterol; induces gene silencing in MCF-7 cells without affe… 5 mg 26585-5 More Info
MHAPC-Chol A cationic cholesterol; induces gene silencing in MCF-7 cells without affe… 500 µg 26585-500 More Info
MHC Class I (human) ELISA Kit Cayman's MHC Class I (human) ELISA Kit is an immunometric assay (i.e. sand… 96 Well 502060-96WELLS More Info
MHY1485 A cell-permeable activator of mTOR that can induce cellular LC3-II accumul… 10 mg 18008-10 More Info
MHY1485 A cell-permeable activator of mTOR that can induce cellular LC3-II accumul… 25 mg 18008-25 More Info
MHY1485 A cell-permeable activator of mTOR that can induce cellular LC3-II accumul… 5 mg 18008-5 More Info
MHY1485 A cell-permeable activator of mTOR that can induce cellular LC3-II accumul… 50 mg 18008-50 More Info
MHY553 An agonist of PPARα; activates PPARα in HepG2 cells in a repor… 1 mg 36088-1 More Info
MHY553 An agonist of PPARα; activates PPARα in HepG2 cells in a repor… 10 mg 36088-10 More Info
MHY553 An agonist of PPARα; activates PPARα in HepG2 cells in a repor… 25 mg 36088-25 More Info
MHY553 An agonist of PPARα; activates PPARα in HepG2 cells in a repor… 5 mg 36088-5 More Info
MHY908 A PPARα and PPARγ dual agonist; increases transcriptional acti… 1 mg 18293-1 More Info
MHY908 A PPARα and PPARγ dual agonist; increases transcriptional acti… 10 mg 18293-10 More Info
MHY908 A PPARα and PPARγ dual agonist; increases transcriptional acti… 5 mg 18293-5 More Info
MHY908 A PPARα and PPARγ dual agonist; increases transcriptional acti… 500 µg 18293-500 More Info
M2I-1 An inhibitor of the Mad2-Cdc20 interaction; inhibits Mad2 binding to Cdc20… 1 mg 22297-1 More Info
M2I-1 An inhibitor of the Mad2-Cdc20 interaction; inhibits Mad2 binding to Cdc20… 10 mg 22297-10 More Info
M2I-1 An inhibitor of the Mad2-Cdc20 interaction; inhibits Mad2 binding to Cdc20… 25 mg 22297-25 More Info
M2I-1 An inhibitor of the Mad2-Cdc20 interaction; inhibits Mad2 binding to Cdc20… 5 mg 22297-5 More Info
MI 2 A MALT1 inhibitor (IC50 = 5.84 µM in a fluorescence assay); inhibits… 1 mg 23437-1 More Info
MI 2 A MALT1 inhibitor (IC50 = 5.84 µM in a fluorescence assay); inhibits… 10 mg 23437-10 More Info
MI 2 A MALT1 inhibitor (IC50 = 5.84 µM in a fluorescence assay); inhibits… 25 mg 23437-25 More Info
MI 2 A MALT1 inhibitor (IC50 = 5.84 µM in a fluorescence assay); inhibits… 5 mg 23437-5 More Info
MI-136 An inhibitor of the menin-MLL interaction (IC50 = 31 nM; Kd = 23.6 nM); bl… 1 mg 19245-1 More Info
MI-136 An inhibitor of the menin-MLL interaction (IC50 = 31 nM; Kd = 23.6 nM); bl… 10 mg 19245-10 More Info
MI-136 An inhibitor of the menin-MLL interaction (IC50 = 31 nM; Kd = 23.6 nM); bl… 25 mg 19245-25 More Info
MI-136 An inhibitor of the menin-MLL interaction (IC50 = 31 nM; Kd = 23.6 nM); bl… 5 mg 19245-5 More Info
MI-192 An HDAC inhibitor that preferentially inhibits HDAC2 (IC50 = 30 nM) and HD… 1 mg 18288-1 More Info
MI-192 An HDAC inhibitor that preferentially inhibits HDAC2 (IC50 = 30 nM) and HD… 10 mg 18288-10 More Info
MI-192 An HDAC inhibitor that preferentially inhibits HDAC2 (IC50 = 30 nM) and HD… 5 mg 18288-5 More Info
MI-2 An inhibitor of menin-MLL fusion protein interactions (IC50 = 446 nM); bin… 10 mg 29218-10 More Info
MI-2 An inhibitor of menin-MLL fusion protein interactions (IC50 = 446 nM); bin… 25 mg 29218-25 More Info
MI-2 An inhibitor of menin-MLL fusion protein interactions (IC50 = 446 nM); bin… 5 mg 29218-5 More Info
MI-2 An inhibitor of menin-MLL fusion protein interactions (IC50 = 446 nM); bin… 50 mg 29218-50 More Info
MI-3 An inhibitor of menin-MLL fusion protein interactions (IC50 = 648 nM); bin… 1 mg 27214-1 More Info
MI-3 An inhibitor of menin-MLL fusion protein interactions (IC50 = 648 nM); bin… 5 mg 27214-5 More Info
MI-3 An inhibitor of menin-MLL fusion protein interactions (IC50 = 648 nM); bin… 500 µg 27214-500 More Info
MI-463 An inhibitor of menin-MLL fusion protein interactions (IC50 = 15 nM); inhi… 1 mg 33525-1 More Info
MI-463 An inhibitor of menin-MLL fusion protein interactions (IC50 = 15 nM); inhi… 10 mg 33525-10 More Info
MI-463 An inhibitor of menin-MLL fusion protein interactions (IC50 = 15 nM); inhi… 25 mg 33525-25 More Info
MI-463 An inhibitor of menin-MLL fusion protein interactions (IC50 = 15 nM); inhi… 5 mg 33525-5 More Info
MI-77301 Binds MDM2 (Ki = 0.88 nM), blocking MDM2-p53 protein-protein interaction,… 1 mg 17473-1 More Info
MI-77301 Binds MDM2 (Ki = 0.88 nM), blocking MDM2-p53 protein-protein interaction,… 10 mg 17473-10 More Info
MI-77301 Binds MDM2 (Ki = 0.88 nM), blocking MDM2-p53 protein-protein interaction,… 5 mg 17473-5 More Info
MI-77301 Binds MDM2 (Ki = 0.88 nM), blocking MDM2-p53 protein-protein interaction,… 500 µg 17473-500 More Info
Mianserin (hydrochloride) An analytical reference standard categorized as an antidepressant; intende… 1 mg 39378-1 More Info
Mianserin (hydrochloride) An analytical reference standard categorized as an antidepressant; intende… 5 mg 39378-5 More Info
Mibefradil (hydrochloride) A general calcium channel blocker that shows modest selectivity for T-type… 10 mg 15037-10 More Info
Mibefradil (hydrochloride) A general calcium channel blocker that shows modest selectivity for T-type… 25 mg 15037-25 More Info
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640

Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com

http://www.caymanchem.com

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