4-(Methylsulfonyl)benzyl+alcohol
Supplier:
BeanTown Chemical
Description:
CAS: 7791-28-8; EC No: 234-140-0; MDL No: MFCD00149153
UN No: UN1564; Haz Class: 6.1; Packing Group: III
Crystalline; Molecular Formula: BaBr2·2H2O; MW: 333.17
Supplier:
BeanTown Chemical
Description:
CAS: 6020-87-7; EC No: 200-306-6; MDL No: MFCD00071582; RTECS: MB7706000
Powder; Molecular Formula: C4H9N3O2·H2O ; MW: 149.15
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
Sodium Hydroxide, 1.0N Solution, Biotech Reagent
Supplier:
Thermo Scientific Chemicals
Description:
Ceftriaxone disodium salt, 50 mg/ml in distilled water
Supplier:
AMBEED, INC
Description:
5-Carboxyfluorescein 97%
Supplier:
Spectrum Chemicals
Description:
Calcium Chloride, Dihydrate, USP, EP, BP, JP is used in treatment of hypocalcemia, electrolyte depletion, and hyperkalemia. All Spectrum Chemical USP, EP, BP, JP grade products are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities
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Supplier:
Strem Chemicals Inc
Description:
CAS #: 7784-13-6. Size: 25g.
Supplier:
BeanTown Chemical
Description:
CAS: 10025-70-4; EC No: 233-971-6; MDL No: MFCD00149865; RTECS: WK8575000
Crystalline; Linear Formula: SrCl2·6H2O ; MW: 266.62
Density (g/mL): 1.93; Refractive Index: 1.650
Hygroscopic
Catalog Number:
(77982-067)
Supplier:
LGC STANDARDS
Description:
(R)-De(trifluoromethyl) Fluoxetine Hydrochloride, TRC, LGC Standards
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
5-Carboxyfluorescein 95%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
2'-Deoxyadenosine monohydrate 99%
Supplier:
Adipogen
Description:
Cell permeable kinase inhibitor with improved selectivity for protein kinase C (PKC) (Ki = 10 nM). Competitive inhibitor for the ATP-binding site of PKC. Anti-inflammatory. Binds to P-glycoprotein. Telomerase activity inhibitor. Potent glycogen synthase kinase-3 (GSK-3) inhibitor. Necrosis inhibitor. Blocks hERG potassium channels. Promotes osteoblastogenesis in human mesenchymal stem cells.
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Supplier:
Honeywell Research Chemicals
Description:
Sodium selenite pentahydrate, Purity: >/= 99.0%, Grade: Puriss. P.a, CAS Number: 26970-82-1, Molecular formula: Na2SeO3.5H2O, Molar mass: 263.01 g/mol, Appearance/color: White to Off White, Size: 100G( glass bottle)
Catalog Number:
(10329-758)
Supplier:
Bioss
Description:
Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoforms USO have no channel activity by themself, but modulates channel characteristics by forming heterotetramers with other isoforms which are retained intracellularly and undergo ubiquitin-dependent degradation.
Catalog Number:
(76080-286)
Supplier:
Bioss
Description:
Receptor for GABA. The activity of this receptor is mediated by G-proteins that inhibit adenylyl cyclase activity, stimulates phospholipase A2, activates potassium channels, inactivates voltage-dependent calcium-channels and modulates inositol phospholipids hydrolysis. Plays a critical role in the fine-tuning of inhibitory synaptic transmission. Pre-synaptic GABA-B-R inhibit neurotransmitter release by down-regulating high-voltage activated calcium channels, whereas postsynaptic GABA-B-R decrease neuronal excitability by activating a prominent inwardly rectifying potassium (Kir) conductance that underlies the late inhibitory postsynaptic potentials. Not only implicated in synaptic inhibition but also in hippocampal long-term potentiation, slow wave sleep, muscle relaxation and antinociception.
Catalog Number:
(10412-976)
Supplier:
Bioss
Description:
Receptor for GABA. The activity of this receptor is mediated by G-proteins that inhibit adenylyl cyclase activity, stimulates phospholipase A2, activates potassium channels, inactivates voltage-dependent calcium-channels and modulates inositol phospholipids hydrolysis. Plays a critical role in the fine-tuning of inhibitory synaptic transmission. Pre-synaptic GABA-B-R inhibit neurotransmitter release by down-regulating high-voltage activated calcium channels, whereas postsynaptic GABA-B-R decrease neuronal excitability by activating a prominent inwardly rectifying potassium (Kir) conductance that underlies the late inhibitory postsynaptic potentials. Not only implicated in synaptic inhibition but also in hippocampal long-term potentiation, slow wave sleep, muscle relaxation and antinociception.
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