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Hai cercato: 3-beta-Hydroxy-delta-5-cholenic+acid


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Codice catalogo: (BOSSBS-12083R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-A555
Codice articolo locale: BOSSBS-12083R-A555
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesized, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawl symptoms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12083R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-A350
Codice articolo locale: BOSSBS-12083R-A350
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesized, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawl symptoms.
UOM: 1 * 100 µl


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Codice catalogo: (BOSSBS-12083R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-FITC
Codice articolo locale: BOSSBS-12083R-FITC
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesized, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawl symptoms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12081R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-12081R-HRP
Codice articolo locale: BOSSBS-12081R-HRP
Descrizione: GAD-65 and GAD-67, glutamate decarboxylases, function to catalyze the production of GABA (gamma-aminobutyric acid). In the central nervous system GABA functions as the main inhibitory transmitter by increasing a Cl- conductance that inhibits neuronal firing. GABA has been shown to activate both ionotropic (GABAA) and metabotropic (GABAB) receptors as well as a third class of receptors called GABAC. Both GABAA and GABAC are ligand-gated ion channels, however, they are structurally and functionally distinct. Members of the GABAA receptor family include GABAA R Alpha 1-6, GABAA R Beta 1-3, GABAA R Gamma 1-3, GABAA R Delta, GABAA R Epsilon, GABAA R Zeta 1 and GABAA R Zeta 2. The GABAB family is composed of GABAB R1 Alpha and GABAB R1 Beta. GABA transporters have also been identified and include GABA T-1, GABA T-2 and GABA T-3 (also designated GAT-1, -2, and -3). The GABA transporters function to terminate GABA action.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12081R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-12081R-A488
Codice articolo locale: BOSSBS-12081R-A488
Descrizione: GAD-65 and GAD-67, glutamate decarboxylases, function to catalyze the production of GABA (gamma-aminobutyric acid). In the central nervous system GABA functions as the main inhibitory transmitter by increasing a Cl- conductance that inhibits neuronal firing. GABA has been shown to activate both ionotropic (GABAA) and metabotropic (GABAB) receptors as well as a third class of receptors called GABAC. Both GABAA and GABAC are ligand-gated ion channels, however, they are structurally and functionally distinct. Members of the GABAA receptor family include GABAA R Alpha 1-6, GABAA R Beta 1-3, GABAA R Gamma 1-3, GABAA R Delta, GABAA R Epsilon, GABAA R Zeta 1 and GABAA R Zeta 2. The GABAB family is composed of GABAB R1 Alpha and GABAB R1 Beta. GABA transporters have also been identified and include GABA T-1, GABA T-2 and GABA T-3 (also designated GAT-1, -2, and -3). The GABA transporters function to terminate GABA action.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12083R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-HRP
Codice articolo locale: BOSSBS-12083R-HRP
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesized, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawl symptoms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12083R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-A750
Codice articolo locale: BOSSBS-12083R-A750
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesised, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawal symptoms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12083R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-CY7
Codice articolo locale: BOSSBS-12083R-CY7
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesized, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawl symptoms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12083R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-12083R-A680
Codice articolo locale: BOSSBS-12083R-A680
Descrizione: Gamma-aminobutyric acid type A (GABAA) receptors mediate inhibitory neurotransmission in the mammalian central nervous system. The receptor exists as a pentameric ion channel composed by heteromeric combinations of alpha, beta, gamma, delta, epsilon, theta, or pi subunits. Only specific subunit combinations produce viable receptors, while others never translocate to the cell surface from the ER where they are synthesised, and subsequently degraded. The theta subunit forms a receptor in combination with alpha3 subunits in monoaminergic cell groups. These receptors, found especially in the septum, preoptic areas, hypothalamic nuclei, amygdala and thalamus, likely have unique pharmacological properties linked to their expression in this particular cell type and not cholinergic cell groups, and may play a role in opiate withdrawal symptoms.
UOM: 1 * 100 µl


Codice catalogo: (TCIAC3134-5MG)
Fornitore: TCI
Codice articolo fornitore: C3134-5MG
Codice articolo locale: TCIAC3134-5MG
Descrizione: N-(9-Cyclopropyl-1-oxononyl)-N-hydroxy-beta-alanine ≥80.0% (by HPLC)
UOM: 1 * 5 mg


Fornitore: Apollo Scientific
Descrizione: Methyl-1-hydroxy-2-naphthoate

Codice catalogo: (TCIAH0797-25G)
Fornitore: TCI
Codice articolo fornitore: H0797-25G
Codice articolo locale: TCIAH0797-25G
Descrizione: Phenyl-1-hydroxy-2-naphthoate ≥98.0% (by GC, titration analysis)
UOM: 1 * 25 g


Fornitore: Thermo Fisher Scientific
Descrizione: Methyl-1-hydroxy-2-naphthoate
Fornitore: Thermo Fisher Scientific
Descrizione: 4-Hydroxy-2(5H)-furanone 96%
Fornitore: Thermo Fisher Scientific
Descrizione: 4-Hydroxy-2(5H)-furanone 95%
Codice catalogo: (APOSOR13802-250MG)
Fornitore: Apollo Scientific
Codice articolo fornitore: OR13802-250MG
Codice articolo locale: APOSOR13802-250MG
Descrizione: 2-Amino-3-hydroxy-3-(4-methoxyphenyl)propanoic acid
UOM: 1 * 250 mg


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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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Puoi ordinare questo prodotto. Se necessario, ti contatteremo per richiedere licenza, autorizzazione o dichiarazione d'uso per procedere con la fornitura.
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