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
|