Brusatol |
A quassinoid with diverse biological activities; active against chloroquin… |
25 mg |
30883-25 |
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Brusatol |
A quassinoid with diverse biological activities; active against chloroquin… |
5 mg |
30883-5 |
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Bryostatin 1 |
A marine macrolide with diverse biological activities; binds to PKCα… |
10 µg |
14802-10 |
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BSA-Arachidonate Polyunsaturated Fatty Acid Complex (1 mM) |
A fatty acid substrate; can be used for efficient fatty acid delivery to c… |
5 mL |
34931-5 |
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BSA Control for BSA-Fatty Acid Complexes (1 mM) |
A control for 1 mM BSA-fatty acid complexes; can be used as a control for… |
5 mL |
34932-5 |
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BSA Control for BSA-Fatty Acid Complexes (5 mM) |
A control for 5 mM BSA-fatty acid complexes; can be used as a control for… |
5 mL |
29556-5 |
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BSA-Docosahexaenoate Polyunsaturated Fatty Acid Complex (1 mM) |
A fatty acid substrate |
5 ml |
35872-5 |
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BSA-γ-Linolenate Polyunsaturated Fatty Acid Complex (1 mM) |
A fatty acid substrate |
5 mL |
39149-5 |
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BSA-Linoleate ω-6 Polyunsaturated Fatty Acid Complex |
A fatty acid substrate; can be used for efficient fatty acid delivery to c… |
5 mL |
38649-5 |
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BSA-Octanoate Saturated Fatty Acid Complex (1 mM) |
A fatty acid substrate; can be used for efficient fatty acid delivery to c… |
5 mL |
34933-5 |
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BSA-Oleate Monounsaturated Fatty Acid Complex (5 mM) |
A fatty acid substrate; has been used for efficient fatty acid delivery to… |
5 mL |
29557-5 |
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BSA-Palmitate Saturated Fatty Acid Complex (5 mM) |
A fatty acid substrate; can be used for efficient fatty acid delivery to c… |
5 mL |
29558-5 |
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BSA-13(Z)-Docosenoate Monounsaturated Fatty Acid Complex (1 mM) |
A fatty acid substrate |
5 mL |
39150-5 |
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BSH-IN-1 |
An inhibitor of bile salt hydrolases; selective for bile salt hydrolases o… |
1 mg |
30311-1 |
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BSH-IN-1 |
An inhibitor of bile salt hydrolases; selective for bile salt hydrolases o… |
5 mg |
30311-5 |
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BSH-IN-1 |
An inhibitor of bile salt hydrolases; selective for bile salt hydrolases o… |
500 µg |
30311-500 |
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BS-181 (hydrochloride) |
A selective Cdk7 inhibitor that blocks the activity of Cdk-activating kina… |
1 mg |
17996-1 |
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BS-181 (hydrochloride) |
A selective Cdk7 inhibitor that blocks the activity of Cdk-activating kina… |
10 mg |
17996-10 |
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BS-181 (hydrochloride) |
A selective Cdk7 inhibitor that blocks the activity of Cdk-activating kina… |
5 mg |
17996-5 |
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BS-181 (hydrochloride) |
A selective Cdk7 inhibitor that blocks the activity of Cdk-activating kina… |
50 mg |
17996-50 |
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BSI-201 |
An irreversible, noncompetitive inhibitor of PARP1 that disrupts binding b… |
10 mg |
11304-10 |
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BSI-201 |
An irreversible, noncompetitive inhibitor of PARP1 that disrupts binding b… |
100 mg |
11304-100 |
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BSI-201 |
An irreversible, noncompetitive inhibitor of PARP1 that disrupts binding b… |
50 mg |
11304-50 |
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BSJ-4-116 |
A PROTAC that drives Cdk12 degradation; induces time- and concentration-de… |
10 mg |
39564-10 |
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BSJ-4-116 |
A PROTAC that drives Cdk12 degradation; induces time- and concentration-de… |
25 mg |
39564-25 |
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BSJ-4-116 |
A PROTAC that drives Cdk12 degradation; induces time- and concentration-de… |
5 mg |
39564-5 |
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BSJ-4-116 |
A PROTAC that drives Cdk12 degradation; induces time- and concentration-de… |
50 mg |
39564-50 |
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BSP-16 |
A STING agonist; binds to STING (Kd = 23 µM); induces the production… |
1 mg |
37992-1 |
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BSP-16 |
A STING agonist; binds to STING (Kd = 23 µM); induces the production… |
5 mg |
37992-5 |
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BSP-16 |
A STING agonist; binds to STING (Kd = 23 µM); induces the production… |
500 µg |
37992-500 |
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BTB06584 |
An inhibitor of mitochondrial F1FO-ATPase; slows ATP consumption following… |
10 mg |
21032-10 |
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BTB06584 |
An inhibitor of mitochondrial F1FO-ATPase; slows ATP consumption following… |
25 mg |
21032-25 |
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BTB06584 |
An inhibitor of mitochondrial F1FO-ATPase; slows ATP consumption following… |
5 mg |
21032-5 |
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BTB06584 |
An inhibitor of mitochondrial F1FO-ATPase; slows ATP consumption following… |
50 mg |
21032-50 |
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BTB-1 |
A reversible Kif18A inhibitor (IC50 = 1.69 µM); selective for Kif18A… |
1 g |
27219-1 |
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BTB-1 |
A reversible Kif18A inhibitor (IC50 = 1.69 µM); selective for Kif18A… |
250 mg |
27219-250 |
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BTB-1 |
A reversible Kif18A inhibitor (IC50 = 1.69 µM); selective for Kif18A… |
500 mg |
27219-500 |
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BTC AM |
A cell-permeable acetoxy-methyl ester of BTC, |
1 mg |
20424-1 |
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BTC (potassium salt) |
A low affinity calcium indicator (Kd = 7-26 µM); ex / em spectra = 4… |
1 mg |
20423-1 |
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BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogeneous TR-FRET ass… |
2400 Well |
500240-2400WELLS |
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BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogeneous TR-FRET ass… |
480 Well |
500240-480WELLS |
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BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogeneous TR-FRET ass… |
4800 Well |
500240-4800WELLS |
More Info
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BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogeneous TR-FRET ass… |
96 Well |
500240-96WELLS |
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BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogeneous TR-FRET ass… |
9600 Well |
500240-9600WELLS |
More Info
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BTK (Total) and BTK (Phospho-Tyr223) TR-FRET Assay Kit |
This BTK (Total) and BTK (Phospho-Tyr223) TR-FRET Assay Kit uses a homogen… |
480 Well |
500242-480WELLS |
More Info
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BTK (Total) TR-FRET Assay Kit |
This BTK (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay method… |
2400 Well |
500241-2400WELLS |
More Info
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BTK (Total) TR-FRET Assay Kit |
This BTK (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay method… |
480 Well |
500241-480WELLS |
More Info
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BTK (Total) TR-FRET Assay Kit |
This BTK (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay method… |
4800 Well |
500241-4800WELLS |
More Info
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BTK (Total) TR-FRET Assay Kit |
This BTK (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay method… |
96 Well |
500241-96WELLS |
More Info
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BTK (Total) TR-FRET Assay Kit |
This BTK (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay method… |
9600 Well |
500241-9600WELLS |
More Info
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