dppiv inhibitor

279  

P32/98 (DPPIV/DPP4 inhibitor)
SIH-385-10MG 10 mg
EUR 185
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
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

Porcine DPPIV ELISA Kit
EPD0261 96Tests
EUR 521

Canine DPPIV ELISA Kit
ECD0261 96Tests
EUR 521

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:

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:

Rat Dipeptidyl Peptldase IV (DPPIV) CLIA Kit
abx196908-96tests 96 tests
EUR 825

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

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

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
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.

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

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

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

Ribonuclease inhibitor
RB0478 5KU
EUR 154.4

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

NFAT Inhibitor
HY-P1026 5mg
EUR 436

XL647Kinase Inhibitor
E1KS1083 5 mg
EUR 873

NADH-Inhibitor
Y4681000 10mg
EUR 200.8

Endotoxin Inhibitor
5-01105 4 x 1mg Ask for price

Kallikrein Inhibitor
5-01416 4 x 5mg Ask for price

Papain Inhibitor
5-01715 10mg Ask for price

Trypsin inhibitor
AG160 1 mg
EUR 523

Trypsin inhibitor
AT160 1mg
EUR 1368

Rinbonuclease Inhibitor
abx098030-10kU 10 kU
EUR 537

Rinbonuclease Inhibitor
abx098030-2kU 2 kU
EUR 425

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].

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?.

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
C3398-25 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?.

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
B1233-50 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.

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
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

NFAT Inhibitor
A4539-1 1 mg
EUR 138
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

NFAT Inhibitor
A4539-10 10 mg
EUR 763
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

NFAT Inhibitor
A4539-5 5 mg
EUR 450
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

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.

Apoptosis Inhibitor
A1930-10 10 mg
EUR 142
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor
A1930-100 100 mg
EUR 456
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor
A1930-25 25 mg
EUR 235
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor
A1930-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Apoptosis Inhibitor
A1930-S Evaluation Sample
EUR 81
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay.

Elastase Inhibitor
A2579-5 5 mg
EUR 166
Description: A potent, irreversible inhibitor of human neutrophil elastase (HNE). The structure of the enzyme-inhibitor complex reveals crosslinking of the catalytic residues His-57 and Ser-195 by the peptidyl chloromethylketone.

BRAF inhibitor
A3263-10 10 mg
EUR 383
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor
A3263-5.1 10 mM (in 1mL DMSO)
EUR 448
Description: BRAF inhibitor is a potent BRAF inhibitor.

BRAF inhibitor
A3263-50 50 mg
EUR 985
Description: BRAF inhibitor is a potent BRAF inhibitor.

CDK9 inhibitor
A3294-10 10 mg
EUR 328
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes.