dppiv inhibitor

279  

DPPIV Inhibitor, P32/98
2571-5
EUR 153

P32/98 (DPPIV/DPP4 inhibitor)
SIH-385-10MG 10 mg
EUR 185
  • P32/98 (Ile-thiazolidide) is a specific, competitive transition-state substrate analog inhibitor of dipeptidyl peptidase IV (DPIV
  • DPPIV
  • CD26), with a Ki of 130 nM (1-3). Useful in diabetes research. Has been used in vivo (10mg/kg orally twice daily
  • Show more
Description: The substance P32/98 is a dppiv/dpp4 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in water (20 mg/ml) or DMSO (25 mg/ml).

P32/98 (DPPIV/DPP4 inhibitor)
SIH-385-50MG 50 mg
EUR 625
  • P32/98 (Ile-thiazolidide) is a specific, competitive transition-state substrate analog inhibitor of dipeptidyl peptidase IV (DPIV
  • DPPIV
  • CD26), with a Ki of 130 nM (1-3). Useful in diabetes research. Has been used in vivo (10mg/kg orally twice daily
  • Show more
Description: The substance P32/98 is a dppiv/dpp4 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in water (20 mg/ml) or DMSO (25 mg/ml).

DPPIV/ Rat DPPIV ELISA Kit
ELA-E0884r 96 Tests
EUR 886

DPPIV (Human) Antibody
6693-50
EUR 457

DPPIV (Mouse) Antibody
6694-50
EUR 457

Polyclonal DPPIV (Human) Antibody
APR07621G 0.05mg
EUR 528
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human DPPIV (Human) . This antibody is tested and proven to work in the following applications:

Polyclonal DPPIV (Mouse) Antibody
APG00005G 0.05mg
EUR 528
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human DPPIV (Mouse) . This antibody is tested and proven to work in the following applications:

Canine DPPIV ELISA Kit
ECD0261 96Tests
EUR 521

Porcine DPPIV ELISA Kit
EPD0261 96Tests
EUR 521

Rat Dipeptidyl Peptldase IV (DPPIV) CLIA Kit
abx196908-96tests 96 tests
EUR 825
  • Shipped within 5-12 working days.

Human CellExp? DPPIV/CD26, human recombinant (untagged)
7436-10
EUR 414

Recombinant DPPIV Protein (Asn 29-Pro 766)
VAng-1468Lsx-1mg 1 mg
EUR 7749
Description: Human DPPIV is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

Recombinant DPPIV Protein (Asn 29-Pro 766)
VAng-1468Lsx-50g 50 µg
EUR 1178
Description: Human DPPIV is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

DPPIV ELISA Kit (Human) : 96 Wells (OKAG00222)
OKAG00222 96 Wells
EUR 596
Description: Description of target: The protein encoded by this gene is identical to adenosine deaminase complexing protein-2, and to the T-cell activation antigen CD26. It is an intrinsic membrane glycoprotein and a serine exopeptidase that cleaves X-proline dipeptides from the N-terminus of polypeptides.;Species reactivity: Human;Application: ELISA;Assay info: Quantitative Colorimentric Sandwich ELISA;Sensitivity: 32 pg/mL

Recombinant DPPIV Protein (Asn 29-Pro 766) [Fc]
VAng-1469Lsx-1mg 1 mg
EUR 4999
Description: Human DPPIV, Fc tag, is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

Recombinant DPPIV Protein (Asn 29-Pro 766) [Fc]
VAng-1469Lsx-50g 50 µg
EUR 985
Description: Human DPPIV, Fc tag, is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

Recombinant DPPIV Protein (Asp 34-Pro 766) [His]
VAng-1470Lsx-200g 200 µg
EUR 1755
Description: Human DPPIV, His tag, is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

Recombinant DPPIV Protein (Asp 34-Pro 766) [His]
VAng-1470Lsx-50g 50 µg
EUR 985
Description: Human DPPIV, His tag, is expressed in HEK 293 cells. (Uniprot ID: NP_001926.2)

Ribunuclease Inhibitor / RNase Inhibitor
105-310 2000 u
EUR 76

Ribunuclease Inhibitor / RNase Inhibitor
105-350 10000 u
EUR 237

MAPKII Kinase Inhibitor (Hsp25 Kinase Inhibitor)
SIH-120A 1 mg
EUR 179
  • The MAPK (mitogen activated protein kinase) comprises a family of ubiquitous praline-directed, protein serine/threonine kinases which signal transduction pathways that control intracellular events including acute responses to hormones and major devel
  • Show more
Description: The substance MAPKII Kinase Inhibitor is a hsp25 kinase inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is white solid which is soluble in DMSO or H20.

Trypsin inhibitor
AG160 1 mg
EUR 523

STAT5 Inhibitor
C4105-10 10 mg
EUR 196
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor
C4105-25 25 mg
EUR 376
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

STAT5 Inhibitor
C4105-5 5 mg
EUR 126
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1].

PKR Inhibitor
C4439-10 10 mg
EUR 206
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

PKR Inhibitor
C4439-25 25 mg
EUR 398
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

PKR Inhibitor
C4439-5 5 mg
EUR 137
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions.

PI3K-? Inhibitor
B1869-25
EUR 675

PI3K-? Inhibitor
B1869-5
EUR 207

PKM2 Inhibitor
B2593-25
EUR 631

PKM2 Inhibitor
B2593-5
EUR 196

CDK4 inhibitor
B1233-10 10 mg
EUR 469
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor
B1233-100 100 mg
EUR 1592
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor
B1233-25 25 mg
EUR 656
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor
B1233-5 5 mg
EUR 325
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

CDK4 inhibitor
B1233-50 50 mg
EUR 1041
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family.

Trypsin inhibitor
AT160 1mg
EUR 1368

EGFR Inhibitor
C3327-1 1 mg
EUR 154
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor
C3327-25 25 mg
EUR 1146
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

EGFR Inhibitor
C3327-5 5 mg
EUR 363
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

CBF? Inhibitor
C3398-10 10 mg
EUR 203
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CBF? Inhibitor
C3398-25 25 mg
EUR 393
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

CBF? Inhibitor
C3398-5 5 mg
EUR 131
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?.

XL647Kinase Inhibitor
E1KS1083 5 mg
EUR 873

BRAF inhibitor
HY-10247 10mM/1mL
EUR 354

PLpro inhibitor
HY-17542 5mg
EUR 533

CPA inhibitor
HY-70005 50mg
EUR 1297

Neurotoxin Inhibitor
HY-112722 10mM/1mL
EUR 744

Lck Inhibitor
HY-12072 100mg
EUR 2019

MEK inhibitor
HY-12202 5mg
EUR 429

Nav1.7 inhibitor
HY-13985 10mM/1mL
EUR 580

NFAT Inhibitor
H-4874.0500 0.5mg
EUR 273
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net

NFAT Inhibitor
H-4874.1000 1.0mg
EUR 454
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net

Endotoxin Inhibitor
H-1382.0001 1.0mg
EUR 113
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9]

Endotoxin Inhibitor
H-1382.0005 5.0mg
EUR 318
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9]

NFAT Inhibitor
HY-P1026 5mg
EUR 436

DDR Inhibitor
HY-W018931 10mM/1mL
EUR 998

Rinbonuclease Inhibitor
abx098030-10kU 10 kU
EUR 537
  • Shipped within 5-10 working days.

Rinbonuclease Inhibitor
abx098030-2kU 2 kU
EUR 425
  • Shipped within 5-10 working days.

Stat5 Inhibitor
9484-1
EUR 120

Stat5 Inhibitor
9484-5
EUR 327

Papain Inhibitor
A1035-25 25 mg
EUR 90
Description: Papain Inhibitor peptide,(C19H29N7O6),a peptide with the sequence H-Gly-Gly-Tyr-Arg-OH,MW= 451.4,this peptide Inhibits the peptidase activity of Papain.

MEK inhibitor
A3594-10 10 mg
EUR 746
Description: A potent MEK inhibitor, Antitumor agent.

MEK inhibitor
A3594-5 5 mg
EUR 547
Description: A potent MEK inhibitor, Antitumor agent.

MEK inhibitor
A3594-5.1 10 mM (in 1mL DMSO)
EUR 598
Description: A potent MEK inhibitor, Antitumor agent.

PDK1 inhibitor
A3706-10 10 mg
EUR 495
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

PDK1 inhibitor
A3706-100 100 mg
EUR 2583
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.

PDK1 inhibitor
A3706-5 5 mg
EUR 290
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM.