MC-Easy Minicircle DNA Production Kit (does not include ZYCY10P3S2T producer E. coli strain)
MN915A-1 10 preps
EUR 1297
  • Category: Minicircle Technology
JNK-IN-8
2729-100 Ask for price
JNK-IN-8
2729-25
EUR 697
JNK-IN-8
2729-5
EUR 218
Mps1-IN-1
B1603-25
EUR 838
Mps1-IN-1
B1603-5
EUR 251
JNK-IN-7
B1695-1
EUR 185
JNK-IN-7
B1695-5
EUR 588
TLR2-IN-C29
B2121-25
EUR 756
TLR2-IN-C29
B2121-5
EUR 229
DprE1-IN-2
B2295-25
EUR 675
DprE1-IN-2
B2295-5
EUR 207
IDO-IN-2
B2496-25
EUR 631
IDO-IN-2
B2496-5
EUR 196
Kif15-IN-1
B3280-10 10 mg
EUR 644
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-100 100 mg
EUR 2541
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-1000 1 g
EUR 10359
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-5 5 mg
EUR 464
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-50 50 mg
EUR 1830
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-S Evaluation Sample
EUR 81
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-10 10 mg
EUR 954
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-100 100 mg
EUR 3850
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-5 5 mg
EUR 683
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-50 50 mg
EUR 2764
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
DDR1-IN-1
B3383-10 10 mg
EUR 311
Description: DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50/EC50 of 105 nM/87 nM; 4-fold less potent for DDR2 (IC50= 413 nM).
DDR1-IN-1
B3383-5 5 mg
EUR 206
Description: DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50/EC50 of 105 nM/87 nM; 4-fold less potent for DDR2 (IC50= 413 nM).
DUBs-IN-2
B3515-10 10 mg
EUR 954
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-100 100 mg
EUR 3850
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-5 5 mg
EUR 683
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-5.1 10 mM (in 1mL DMSO)
EUR 746
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-50 50 mg
EUR 2764
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-3
B3516-10 10 mg
EUR 954
DUBs-IN-3
B3516-100 100 mg
EUR 3850
DUBs-IN-3
B3516-5 5 mg
EUR 683
DUBs-IN-3
B3516-50 50 mg
EUR 2764
CDK7-IN-1
B4665-1 1 mg
EUR 358
IKK?-IN-1
B4825-10 10 mg
EUR 954
IKK?-IN-1
B4825-100 100 mg
EUR 3850
IKK?-IN-1
B4825-5 5 mg
EUR 683
IKK?-IN-1
B4825-5.1 10 mM (in 1mL DMSO)
EUR 746
IKK?-IN-1
B4825-50 50 mg
EUR 2764
Mps1-IN-1
B4907-10 10 mg
EUR 221
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-5 5 mg
EUR 144
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-5.1 10 mM (in 1mL DMSO)
EUR 212
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-50 50 mg
EUR 656
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-2
B1138-10 10 mg
EUR 293
Description: Mps1-IN-2 is a potent and selective ATP-competitive inhibitor of Mps1 kinase with the IC50 value of 145nM [1].Mps1-IN-2 has been reported to inhibit Mps1 kinase activity with the IC50 value of 145nM, when screened at 1?M ATP.
Mps1-IN-2
B1138-25 25 mg
EUR 572
Description: Mps1-IN-2 is a potent and selective ATP-competitive inhibitor of Mps1 kinase with the IC50 value of 145nM [1].Mps1-IN-2 has been reported to inhibit Mps1 kinase activity with the IC50 value of 145nM, when screened at 1?M ATP.
Mps1-IN-2
B1138-5 5 mg
EUR 180
Description: Mps1-IN-2 is a potent and selective ATP-competitive inhibitor of Mps1 kinase with the IC50 value of 145nM [1].Mps1-IN-2 has been reported to inhibit Mps1 kinase activity with the IC50 value of 145nM, when screened at 1?M ATP.
Nampt-IN-1
B1171-25
EUR 675
Nampt-IN-1
B1171-5
EUR 207
BMX-IN-1
B1330-25
EUR 1191
BMX-IN-1
B1330-5
EUR 349
DDR1-IN-1
B1331-25
EUR 675
DDR1-IN-1
B1331-5
EUR 218
Jnk-In-7
20-abx184143
  • EUR 954.00
  • EUR 634.00
  • 10 mg
  • 5 mg
  • Shipped within 1-2 weeks.
IDO-IN-1
C3211-1 1 mg
EUR 139
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
IDO-IN-1
C3211-10 10 mg
EUR 773
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
IDO-IN-1
C3211-5 5 mg
EUR 457
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
BMX-IN-1
A3260-10 10 mg
EUR 398
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-100 100 mg
EUR 1674
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-2 2 mg
EUR 160
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-5 5 mg
EUR 247
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-5.1 10 mM (in 1mL DMSO)
EUR 427
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-50 50 mg
EUR 1198
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
JNK-IN-7
A3519-10 10 mg
EUR 477
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-100 100 mg
EUR 1892
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-5 5 mg
EUR 383
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-5.1 10 mM (in 1mL DMSO)
EUR 415
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-50 50 mg
EUR 1207
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-8
A3520-10 10 mg
EUR 258
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-5 5 mg
EUR 189
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-5.1 10 mM (in 1mL DMSO)
EUR 226
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-50 50 mg
EUR 676
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
LRRK2-IN-1
A3558-10 10 mg
EUR 148
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.
LRRK2-IN-1
A3558-100 100 mg
EUR 595
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.