PcrSb For Hpv

Lab Reagents

Hpv Pcr Laboratories manufactures the pcr/sb for hpv reagents distributed by Genprice. The Pcr/Sb For Hpv reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact HPV PCR. Other Pcr/Sb products are available in stock. Specificity: Pcr/Sb Category: For Group: Hpv

Hpv information

SB 203580
A8254-25 25 mg
EUR 146.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-250 250 mg
EUR 452.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-50 50 mg
EUR 176.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-S Evaluation Sample
EUR 97.2
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 239063
A3792-25 25 mg
EUR 544.8
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB 239063
A3792-5 5 mg
EUR 196.8
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB 239063
A3792-5.1 10 mM (in 1mL DMSO)
EUR 228
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB-222200
A3795-10 10 mg
EUR 240
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-222200
A3795-5.1 10 mM (in 1mL DMSO)
EUR 258
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-222200
A3795-50 50 mg
EUR 841.2
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-674042
A3800-10 10 mg
EUR 350.4
Description: SB-674042 is a specific, high-affinity OX1 selective antagonist.

SB-674042
A3800-25 25 mg
EUR 717.6
Description: SB-674042 is a specific, high-affinity OX1 selective antagonist.

SB-674042
A3800-5 5 mg
EUR 216
Description: SB-674042 is a specific, high-affinity OX1 selective antagonist.

Sb 431542
20-abx182645
  • EUR 1796.40
  • EUR 444.00
  • 100 mg
  • 10 mg

SB 204070
B5105-10 10 mg
EUR 486

SB 265610
B5333-1 1 mg
EUR 192
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.