A1006 Apexbio

EZ-DNA Reagents
BS8202 100preps
EUR 105.67

Apexbio Reagents Laboratories manufactures the a1006 apexbio reagents distributed by Genprice. The A1006 Apexbio 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 Apexbio Reagents. Other A1006 products are available in stock. Specificity: A1006 Category: Apexbio

PeliKine tool set, additional reagents
1 unit
EUR 177.88

True north Cryobox 0.2mLNatural
PK10
EUR 172.8

True north Cryobox 0.5mLNatural
PK10
EUR 153.6

True north Cryobox1.5/2mLNatural
PK10
EUR 100.8

True north Cryobox 5mLNatural
PK10
EUR 153.6

True north Cryobox 5mLBlue
PK10
EUR 153.6

True north Cryobox 15mLNatural
PK10
EUR 212.4

Human Samples information

A-317491
A3134-10 10 mg
EUR 271.2
Description: A-317491 is a high-affinity and selective antagonist of P2X2/3 and P2X3 receptors with Ki values of 9 and 22 nM, respectively for human P2X2/3 and P2X3 [1].The P2X3 receptor is an ATP-sensitive ligand-gated ion channel expressed on sensory afferent neurons.

A-317491
A3134-25 25 mg
EUR 559.2
Description: A-317491 is a high-affinity and selective antagonist of P2X2/3 and P2X3 receptors with Ki values of 9 and 22 nM, respectively for human P2X2/3 and P2X3 [1].The P2X3 receptor is an ATP-sensitive ligand-gated ion channel expressed on sensory afferent neurons.

A-317491
A3134-5 5 mg
EUR 201.6
Description: A-317491 is a high-affinity and selective antagonist of P2X2/3 and P2X3 receptors with Ki values of 9 and 22 nM, respectively for human P2X2/3 and P2X3 [1].The P2X3 receptor is an ATP-sensitive ligand-gated ion channel expressed on sensory afferent neurons.

A-317491
A3134-50 50 mg
EUR 774
Description: A-317491 is a high-affinity and selective antagonist of P2X2/3 and P2X3 receptors with Ki values of 9 and 22 nM, respectively for human P2X2/3 and P2X3 [1].The P2X3 receptor is an ATP-sensitive ligand-gated ion channel expressed on sensory afferent neurons.

A-443654
A3135-5 5 mg
EUR 559.2
Description: A-443654 is a potent and selective inhibitor of Akt with Ki value of 160 pM [1].The Akt kinases play important roles in cellular signal transduction and take participate in the regulation of cell transformation and tumor progression.

A-443654
A3135-5.1 10 mM (in 1mL DMSO)
EUR 699.6
Description: A-443654 is a potent and selective inhibitor of Akt with Ki value of 160 pM [1].The Akt kinases play important roles in cellular signal transduction and take participate in the regulation of cell transformation and tumor progression.

A-740003
A3136-100 100 mg
EUR 216
Description: A-740003 is a selective and competitive antagonist of P2X7 receptor with IC50 values of 40 nM and 18 nM in human and rat, respectively [1]. P2X7 receptors are members of ATP-sensitive ionotropic P2X receptor family (P2X1?P2X7).

A-740003
A3136-5.1 10 mM (in 1mL DMSO)
EUR 164.4
Description: A-740003 is a selective and competitive antagonist of P2X7 receptor with IC50 values of 40 nM and 18 nM in human and rat, respectively [1]. P2X7 receptors are members of ATP-sensitive ionotropic P2X receptor family (P2X1?P2X7).

A-740003
A3136-50 50 mg
EUR 157.2
Description: A-740003 is a selective and competitive antagonist of P2X7 receptor with IC50 values of 40 nM and 18 nM in human and rat, respectively [1]. P2X7 receptors are members of ATP-sensitive ionotropic P2X receptor family (P2X1?P2X7).

A-867744
A3138-10 10 mg
EUR 351.6
Description: Targeting ?7 neuronal acetylcholine receptors (nAChRs) with selective agonists and positive allosteric modulators (PAMs) is considered a therapeutic approach for managing cognitive deficits in schizophrenia and Alzheimer?s disease.

A-867744
A3138-100 100 mg
EUR 2314.8
Description: Targeting ?7 neuronal acetylcholine receptors (nAChRs) with selective agonists and positive allosteric modulators (PAMs) is considered a therapeutic approach for managing cognitive deficits in schizophrenia and Alzheimer?s disease.

A-867744
A3138-5.1 10 mM (in 1mL DMSO)
EUR 381.6
Description: Targeting ?7 neuronal acetylcholine receptors (nAChRs) with selective agonists and positive allosteric modulators (PAMs) is considered a therapeutic approach for managing cognitive deficits in schizophrenia and Alzheimer?s disease.

A-867744
A3138-50 50 mg
EUR 1340.4
Description: Targeting ?7 neuronal acetylcholine receptors (nAChRs) with selective agonists and positive allosteric modulators (PAMs) is considered a therapeutic approach for managing cognitive deficits in schizophrenia and Alzheimer?s disease.

A-769662
A3963-10 10 mg
EUR 150
Description: A-769662 is a potent activator of AMPK with EC50 value of 0.8 ?M in vitro[1].AMPK(AMP-activated protein kinase) is a serine/threonine protein kinase which is formed by three proteins: ?,? and ? subunits. They play important roles in both the activity and stabilities of AMPK.

A-769662
A3963-25 25 mg
EUR 254.4
Description: A-769662 is a potent activator of AMPK with EC50 value of 0.8 ?M in vitro[1].AMPK(AMP-activated protein kinase) is a serine/threonine protein kinase which is formed by three proteins: ?,? and ? subunits. They play important roles in both the activity and stabilities of AMPK.

A-769662
A3963-5.1 10 mM (in 1mL DMSO)
EUR 157.2
Description: A-769662 is a potent activator of AMPK with EC50 value of 0.8 ?M in vitro[1].AMPK(AMP-activated protein kinase) is a serine/threonine protein kinase which is formed by three proteins: ?,? and ? subunits. They play important roles in both the activity and stabilities of AMPK.

A-769662
A3963-50 50 mg
EUR 421.2
Description: A-769662 is a potent activator of AMPK with EC50 value of 0.8 ?M in vitro[1].AMPK(AMP-activated protein kinase) is a serine/threonine protein kinase which is formed by three proteins: ?,? and ? subunits. They play important roles in both the activity and stabilities of AMPK.