PD-0325901

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
  • EUR 380.40
  • EUR 402.00
  • 100ug
  • 50ug
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
  • EUR 493.20
  • EUR 2214.00
  • EUR 718.80
  • EUR 218.40
  • EUR 360.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

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
  • EUR 4101.60
  • EUR 393.60
  • EUR 276.00
  • 1 mg
  • 20 ug
  • 5 ug

PD-L1 Protein

20-abx263458
  • EUR 1930.80
  • EUR 393.60
  • EUR 276.00
  • 100 ug
  • 10 ug
  • 2 µg

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
  • EUR 733.20
  • EUR 370.80
  • EUR 2192.40
  • EUR 1126.80
  • EUR 1461.60
  • EUR 476.40
  • 100ug
  • 10ug
  • 1MG
  • 200ug
  • 500ug
  • 50ug
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
  • EUR 493.20
  • EUR 2214.00
  • EUR 718.80
  • EUR 218.40
  • EUR 360.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Ribosome-inactivating protein PD-L1 / PD-L2 Antibody (FITC)

20-abx319447
  • EUR 493.20
  • EUR 2214.00
  • EUR 718.80
  • EUR 218.40
  • EUR 360.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

PD-0325901