PD-0325901
To Order Contact us: lieven@wlsolutions.be
Nitrogen-Phosphorus Pesticides Mix D |
||
5252-PD | 1ML | EUR 328.32 |
PD-1/PD-L1 Inhibitor 2 |
||
B1050-25 | EUR 679.2 |
PD-1/PD-L1 Inhibitor 2 |
||
B1050-5 | EUR 242.4 |
PD-1/PD-L1 Inhibitor 1 |
||
B1213-25 | EUR 679.2 |
PD-1/PD-L1 inhibitor 2 |
||
B6023-25 | 25 mg | EUR 525.6 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
PD-1/PD-L1 inhibitor 2 |
||
B6023-5 | 5 mg | EUR 205.2 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
PD-1/PD-L1 inhibitor 1 |
||
B6172-25 | 25 mg | EUR 543.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
PD-1/PD-L1 inhibitor 1 |
||
B6172-5 | 5 mg | EUR 201.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
PD 180970 |
||
A8606-10 | 10 mg | EUR 517.2 |
Description: ATP-competitive inhibitor of p210bcr/abl tyrosine kinase; selectively induces apoptosis in chronic myeloid leukemia (CML) K562 cells. Inhibits in vivo tyrosine phosphorylation of Gab2, CrkL and p210bcr/abl (IC50 values are 80, 80 and 170 nM respectively). |
PD 169316 |
||
A8689-10 | 10 mg | EUR 195.6 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 169316 |
||
A8689-5.1 | 10 mM (in 1mL DMSO) | EUR 268.8 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 169316 |
||
A8689-50 | 50 mg | EUR 595.2 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 145305 |
||
C5830-10 | 10 mg | EUR 513.6 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
PD 145305 |
||
C5830-5 | 5 mg | EUR 315.6 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
PD 0332991 |
||
E1KS1116 | 5mg | EUR 812.4 |
PD 184161 |
||
C4361-10 | 10 mg | EUR 339.6 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 184161 |
||
C4361-25 | 25 mg | EUR 673.2 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 184161 |
||
C4361-5 | 5 mg | EUR 217.2 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 166326 |
||
C3677-1 | 1 mg | EUR 193.2 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 166326 |
||
C3677-10 | 10 mg | EUR 1128 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 166326 |
||
C3677-5 | 5 mg | EUR 661.2 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 150,606 |
||
1906-25 | EUR 444 |
PD 150,606 |
||
1906-5 | EUR 164.4 |
PD 98059 |
||
1666-5 | EUR 189.6 |
PD 173074 |
||
1675-1 | EUR 164.4 |
PD 173074 |
||
1675-100 | Ask for price |
PD 150606 |
||
A4413-25 | 25 mg | EUR 513.6 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
PD 150606 |
||
A4413-5 | 5 mg | EUR 172.8 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
PD 166793 |
||
A4438-10 | 10 mg | EUR 290.4 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 166793 |
||
A4438-25 | 25 mg | EUR 597.6 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 166793 |
||
A4438-5 | 5 mg | EUR 224.4 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 173074 |
||
A8253-10 | 10 mg | EUR 129.6 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
||
A8253-5.1 | 10 mM (in 1mL DMSO) | EUR 142.8 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
||
A8253-50 | 50 mg | EUR 254.4 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
||
A8253-S | Evaluation Sample | EUR 97.2 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD-146176 |
||
B2313-25 | EUR 810 |
PD-146176 |
||
B2313-5 | EUR 248.4 |
PD-168393 |
||
B2352-25 | EUR 496.8 |
PD-168393 |
||
B2352-5 | EUR 170.4 |
PD 151746 |
||
B4791-100 | 100 mg | EUR 714 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
||
B4791-25 | 25 mg | EUR 338.4 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
||
B4791-5 | 5 mg | EUR 142.8 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
||
B4791-5.1 | 10 mM (in 1mL DMSO) | EUR 151.2 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 334581 |
||
B5727-10 | 10 mg | EUR 583.2 |
PD 334581 |
||
B5727-50 | 50 mg | EUR 2220 |
PD 81723 |
||
B6705-10 | 10 mg | EUR 340.8 |
PD 81723 |
||
B6705-50 | 50 mg | EUR 1245.6 |
PD 102807 |
||
B6821-10 | 10 mg | EUR 466.8 |
PD 102807 |
||
B6821-50 | 50 mg | EUR 1771.2 |
PD 160170 |
||
B6972-10 | 10 mg | EUR 408 |
PD 169316 |
||
B1703-25 | EUR 652.8 |
PD 169316 |
||
B1703-5 | EUR 210 |
PD-166866 |
||
B2223-25 | EUR 810 |
PD-166866 |
||
B2223-5 | EUR 248.4 |
PD 176252 |
||
B7122-10 | 10 mg | EUR 614.4 |
PD 198306 |
||
B7124-1 | 1 mg | EUR 151.2 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 198306 |
||
B7124-10 | 10 mg | EUR 634.8 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 198306 |
||
B7124-5 | 5 mg | EUR 381.6 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 135158 |
||
B7127-10 | 10 mg | EUR 583.2 |
PD 135158 |
||
B7127-50 | 50 mg | EUR 2220 |
PD 158780 |
||
B7130-10 | 10 mg | EUR 278.4 |
PD 158780 |
||
B7130-25 | 25 mg | EUR 543.6 |
PD 158780 |
||
B7130-5 | 5 mg | EUR 181.2 |
PD 118057 |
||
B7203-10 | 10 mg | EUR 400.8 |
PD 118057 |
||
B7203-50 | 50 mg | EUR 1491.6 |
PD 146176 |
||
B7208-10 | 10 mg | EUR 180 |
PD 146176 |
||
B7208-25 | 25 mg | EUR 344.4 |
PD 146176 |
||
B7208-50 | 50 mg | EUR 567.6 |
PD 173212 |
||
B7424-10 | 10 mg | EUR 634.8 |
PD 173212 |
||
B7424-5 | 5 mg | EUR 451.2 |
PD 173212 |
||
B7424-5.1 | 10 mM (in 1mL DMSO) | EUR 574.8 |
PD 161570 |
||
B7486-10 | 10 mg | EUR 544.8 |
PD 161570 |
||
B7486-50 | 50 mg | EUR 2056.8 |
PD 98,059 |
||
GK2140-10MG | 10 mg | EUR 206.4 |
PD 98,059 |
||
GK2140-1MG | 1 mg | EUR 109.2 |
PD 98,059 |
||
GK2140-50MG | 50 mg | EUR 453.6 |
PD 98,059 |
||
GK2140-5MG | 5 mg | EUR 164.4 |
PD 150,606 |
||
GL2543-25MG | 25 mg | EUR 495.6 |
PD 150,606 |
||
GL2543-5MG | 5 mg | EUR 184.8 |
PD-159020 |
||
HY-101598 | 1mg | EUR 1350 |
PD 123319 |
||
HY-10259 | 5mg | EUR 218.4 |
PD 169316 |
||
HY-10578 | 10mM/1mL | EUR 306 |
PD 90780 |
||
HY-110166 | 5mg | EUR 391.2 |
PD 407824 |
||
HY-18961 | 100mg | EUR 1850.4 |
PD 151746 |
||
HY-19749 | 50mg | EUR 589.2 |
PD-ECGF |
||
GT15181 | 100 ug | EUR 631.2 |
PD 117519 |
||
HY-100032 | 5mg | EUR 142.8 |
PD-166866 |
||
HY-101296 | 10mM/1mL | EUR 165.6 |
PD-ECGF |
||
PR15044 | 10 ug | EUR 584.4 |
Ribosome-inactivating protein PD-L1/PD-L2 Antibody |
||
1-CSB-PA306294LA01PJJ |
|
|
Description: A polyclonal antibody against Ribosome-inactivating protein PD-L1/PD-L2. Recognizes Ribosome-inactivating protein PD-L1/PD-L2 from Phytolacca dioica. This antibody is Unconjugated. Tested in the following application: ELISA |
Ribosome-inactivating protein PD-L1 / PD-L2 Antibody |
||
20-abx319445 |
|
|
Anti-PD-L1 |
||
DB-241-0.1 | 100 μl | EUR 469.2 |
Description: rabbit monospecific clonal antibodies for ihc-p application; concentrated |
Anti-PD-L1 |
||
DB-241-0.2 | 200 μl | EUR 675.6 |
Description: rabbit monospecific clonal antibodies for ihc-p application; concentrated |
Anti-PD-L1 |
||
DB-241-0.5 | 500 μl | EUR 889.2 |
Description: rabbit monospecific clonal antibodies for ihc-p application; concentrated |
Anti-PD-L1 |
||
DB-241-1 | 1 ml | EUR 1450.8 |
Description: rabbit monospecific clonal antibodies for ihc-p application; concentrated |
Anti-PD-L1 |
||
DB-241-RTU-15 | 15 ml | EUR 813.6 |
Description: rabbit monospecific clonal antibodies for ihc-p application; prediluted (ready to use) |
Anti-PD-L1 |
||
DB-241-RTU-7 | 7 ml | EUR 519.6 |
Description: rabbit monospecific clonal antibodies for ihc-p application; prediluted (ready to use) |
Anti-PD-L1 |
||
DB241-RTU-15 | 15 ml | EUR 813.6 |
Description: rabbit monospecific clonal antibodies for ihc-p application; prediluted (ready to use) |
Anti-PD-L1 |
||
DB241-RTU-7 | 7 ml | EUR 519.6 |
Description: rabbit monospecific clonal antibodies for ihc-p application; prediluted (ready to use) |
PD-L1 Antibody |
||
49251-100ul | 100ul | EUR 399.6 |
PD-L1 Antibody |
||
49251-50ul | 50ul | EUR 286.8 |
PD-L1 Peptide |
||
46-156P | 0.1 mg | EUR 405.6 |
Description: CD274 / PD-L1 Peptide |
PD-L1 Antibody |
||
4059-002mg | 0.02 mg | EUR 206.18 |
Description: PD-L1 plays a critical role in induction and maintenance of immune tolerance to self. As a ligand for the inhibitory receptor PDCD1/CD279, PD-L1 modulates the activation threshold of T-cells and limits T-cell effector response (1). The PDCD1/CD279-mediated inhibitory pathway is exploited by tumors to attenuate anti-tumor immunity and facilitate tumor survival (2,3). Through a yet unknown activating receptor, it may costimulate T-cell subsets that predominantly produce interleukin-10 (IL10) (4). |
PD-L1 Antibody |
||
4059-01mg | 0.1 mg | EUR 523.7 |
Description: PD-L1 plays a critical role in induction and maintenance of immune tolerance to self. As a ligand for the inhibitory receptor PDCD1/CD279, PD-L1 modulates the activation threshold of T-cells and limits T-cell effector response (1). The PDCD1/CD279-mediated inhibitory pathway is exploited by tumors to attenuate anti-tumor immunity and facilitate tumor survival (2,3). Through a yet unknown activating receptor, it may costimulate T-cell subsets that predominantly produce interleukin-10 (IL10) (4). |
PD-L1 Peptide |
||
4059P | 0.05 mg | EUR 197.7 |
Description: (IN) PD-L1 peptide |
PD-L2 Antibody |
||
4063-002mg | 0.02 mg | EUR 206.18 |
Description: PD-L2 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by co gnate peptides bound to MHC molecules on antigen-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PD-L1 and PD-L2, both of which are thought act as a negative regulator of T cell activation. However, it has been suggested that PD-L2 can act to stimulate an immunogenic response through and alternative receptor from PD-1. |
PD-L2 Antibody |
||
4063-01mg | 0.1 mg | EUR 523.7 |
Description: PD-L2 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by co gnate peptides bound to MHC molecules on antigen-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PD-L1 and PD-L2, both of which are thought act as a negative regulator of T cell activation. However, it has been suggested that PD-L2 can act to stimulate an immunogenic response through and alternative receptor from PD-1. |
PD-L2 Peptide |
||
4063P | 0.05 mg | EUR 197.7 |
Description: (IN) PD-L2 peptide |
PD-1 Antibody |
||
4065-002mg | 0.02 mg | EUR 206.18 |
Description: PD-1 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by cognate peptides bound to MHC molecules on antig en-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PDL-1 and PDL-2. Upon binding to either of these ligands, signals generated by PD-1 inhibit the activation of the immune response in the absence of "danger signals" such as LPS or other molecules associated with bacteria or other pathogens. Evidence for this is seen in PD1-null mice who exhibit hyperactivated immune systems and autoimmune diseases. |
PD-1 Antibody |
||
4065-01mg | 0.1 mg | EUR 523.7 |
Description: PD-1 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by cognate peptides bound to MHC molecules on antig en-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PDL-1 and PDL-2. Upon binding to either of these ligands, signals generated by PD-1 inhibit the activation of the immune response in the absence of "danger signals" such as LPS or other molecules associated with bacteria or other pathogens. Evidence for this is seen in PD1-null mice who exhibit hyperactivated immune systems and autoimmune diseases. |
PD-1 Peptide |
||
4065P | 0.05 mg | EUR 197.7 |
Description: (CT) PD-1 peptide |
PD-1 Antibody |
||
4067-002mg | 0.02 mg | EUR 206.18 |
Description: PD-1 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by cognate peptides bound to MHC molecules on antig en-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PDL-1 and PDL-2. Upon binding to either of these ligands, signals generated by PD-1 inhibit the activation of the immune response in the absence of "danger signals" such as LPS or other molecules associated with bacteria or other pathogens. Evidence for this is seen in PD1-null mice who exhibit hyperactivated immune systems and autoimmune diseases. |
PD-1 Antibody |
||
4067-01mg | 0.1 mg | EUR 523.7 |
Description: PD-1 Antibody: Cell-mediated immune responses are initiated by T lymphocytes that are themselves stimulated by cognate peptides bound to MHC molecules on antig en-presenting cells (APC). T-cell activation is generally self-limited as activated T cells express receptors such as PD-1 (also known as PDCD-1) that mediate inhibitory signals from the APC. PD-1 can bind two different but related ligands, PDL-1 and PDL-2. Upon binding to either of these ligands, signals generated by PD-1 inhibit the activation of the immune response in the absence of "danger signals" such as LPS or other molecules associated with bacteria or other pathogens. Evidence for this is seen in PD1-null mice who exhibit hyperactivated immune systems and autoimmune diseases. |
PD-1 Peptide |
||
4067P | 0.05 mg | EUR 197.7 |
Description: (IN) PD-1 peptide |
PD-1 Antibody |
||
24505-100ul | 100ul | EUR 468 |
PD-1 Antibody |
||
24506-100ul | 100ul | EUR 468 |
EZSolution? PD 98059 |
||
1783-5 | EUR 189.6 |
PD 153035 Hydrochloride |
||
1656-2 | EUR 189.6 |
PD 123319 ditrifluoroacetate |
||
A3704-10 | 10 mg | EUR 250.8 |
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist. |
PD 123319 ditrifluoroacetate |
||
A3704-25 | 25 mg | EUR 489.6 |
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist. |
PD 123319 ditrifluoroacetate |
||
A3704-5 | 5 mg | EUR 205.2 |
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist. |
PD 123319 ditrifluoroacetate |
||
A3704-50 | 50 mg | EUR 787.2 |
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist. |
PD-L1 Protein |
||
20-abx261703 |
|
|
PD-L1 Protein |
||
20-abx263458 |
|
|
PD-ECGF Antibody |
||
abx236264-100ug | 100 ug | EUR 661.2 |
PD-0332991 isethionate |
||
9480-25 | EUR 652.8 |
PD-0332991 isethionate |
||
9480-5 | EUR 210 |
PD-123319 ditrifluoroacetate |
||
9640-25 | EUR 757.2 |
PD-123319 ditrifluoroacetate |
||
9640-5 | EUR 235.2 |
PD 98059, >99% |
||
BC064-010 | 10mg | EUR 278.4 |
PD 98059, >99% |
||
BC064-025 | 25mg | EUR 360 |
PD 98059, >99% |
||
BC064-050 | 50mg | EUR 537.6 |
PD 168077 maleate |
||
B6578-10 | 10 mg | EUR 362.4 |
PD 168077 maleate |
||
B6578-50 | 50 mg | EUR 1315.2 |
PD-166285 dihydrochloride |
||
B2094-25 | EUR 757.2 |
PD-166285 dihydrochloride |
||
B2094-5 | EUR 235.2 |
PD 144418 oxalate |
||
B7125-10 | 10 mg | EUR 408 |
PD 144418 oxalate |
||
B7125-50 | 50 mg | EUR 1531.2 |
PD 168568 dihydrochloride |
||
B7420-10 | 10 mg | EUR 369.6 |
PD 168568 dihydrochloride |
||
B7420-50 | 50 mg | EUR 1363.2 |
PD 0332991 (Palbociclib) |
||
B7798-25 | 25 mg | EUR 184.8 |
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6. |
PD 0332991 (Palbociclib) |
||
B7798-5 | 5 mg | EUR 129.6 |
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6. |
PD 0332991 (Palbociclib) |
||
B7798-S | Evaluation Sample | EUR 97.2 |
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6. |
PD-1 Antibody |
||
P1001-01m | 0.1m | EUR 198 |
PD-1 Antibody |
||
P1001-1ml | 1ml | EUR 451.2 |
PD-L1 Antibody |
||
P1013-01m | 0.1m | EUR 224.4 |
PD-L1 Antibody |
||
P1013-1ml | 1ml | EUR 807.6 |
PD-1,CD279 |
||
E6TA00107 | 0.1mg | EUR 411.6 |
PD-L1, CD274 |
||
E6TA00108 | 0.1mg | EUR 411.6 |
PD 123319 (ditrifluoroacetate) |
||
HY-10259A | 10mg | EUR 258 |
(+)-PD 128907 hydrochloride |
||
HY-110000 | 50mg | EUR 901.2 |
PD-168077 maleate |
||
HY-21098A | 10mM/1mL | EUR 211.2 |
PD Adaptor Sterile |
||
PIP5086 | PK5 | EUR 31.46 |
PD-L1 Antibody |
||
R31573 | 100 ug | EUR 419 |
PD-L1 Antibody |
||
R33263-100UG | 100 ug | EUR 399 |
Phytolacca dioica Ribosome-inactivating protein PD-L1/PD-L2 |
||
1-CSB-EP306294PJJ |
|
|
Description: Recombinant Phytolacca dioica Ribosome-inactivating protein PD-L1/PD-L2 expressed in E.coli |
Ribosome-inactivating protein PD-L1 / PD-L2 Antibody (HRP) |
||
20-abx319446 |
|
|
Ribosome-inactivating protein PD-L1 / PD-L2 Antibody (FITC) |
||
20-abx319447 |
|
|