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2-Amino-5-fluoro-6-methylpyridine
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2-Amino-5-fluoro-6-methylpyridine
Lieferant:
Thermo Scientific
Beschreibung:
5-Amino-1H-indazol
Lieferant:
FLUOROCHEM
Beschreibung:
2-Aminofluoren
Lieferant:
VARIAN
Beschreibung:
CP-PoraPLOT Amines is a unique column specially designed for the high retention analysis of very volatile amines.
Artikel-Nr:
(REST35002)
Lieferant:
Restek
Hersteller-Artikelnummer::
35002
Lokale Artikelnummer::
REST35002
Beschreibung:
The amine column test mix consists of (C10) decane (0,60 mg/ml), (C12) dodecane (0.60 mg/ml, 1,2-butanediol (0.60 mg/ml), diethanolamine (DEA) (1.20 mg/ml), diethylenetriamine (1.20 mg/ml), 2,6-dimethylaniline (0.60 mg/ml), 2-nonanol (0.60 mg/ml), pyridine(0.60 mg/ml).
VE:
1 * 1 mL
Artikel-Nr:
(BOSSBS-12460R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12460R-HRP
Lokale Artikelnummer::
BOSSBS-12460R-HRP
Beschreibung:
Aldehyde dehydrogenases (ALDHs) mediate NADP+-dependent oxidation of aldehydes into acids during the detoxification of alcohol-derived acetaldehyde; metabolism of corticosteroids, biogenic amines and neurotransmitters; and lipid peroxidation. ALDH1A1, also designated retinal dehydrogenase 1 (RalDH1 or RALDH1), aldehyde dehydrogenase family 1 member A1, aldehyde dehydrogenase cytosolic, ALDHII, ALDH-E1 or ALDH E1, is a retinal dehydrogenase that participates in the biosynthesis of retinoic acid (RA). There are two major liver isoforms of ALDH1 that can localize to cytosolic or mitochondrial space. The ALDH1A2 (RALDH2, RALDH2-T) gene produces three different transcripts and also catalyzes the synthesis of RA from retinaldehyde. ALDH1A3 (ALDH6, RALDH3, ALDH1A6) is a 37 kb gene that consists of 13 exons and produces a major transcript of approximately 3.5 kb most abundant in salivary gland, stomach and kidney. ALDH3A1 (stomach type, ALDH3, ALDHIII) forms a cytoplasmic homodimer that preferentially oxidizes aromatic aldehyde substrates. ALDH genes upregulate as a part of the oxidative stress response, and appear to be abundant in certain tumors that have an accelerated metabolism toward chemotherapy agents.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-A680
Lokale Artikelnummer::
BOSSBS-4176R-A680
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
5-Amino-2-(trifluormethyl)pyridin
Lieferant:
Sigma-Aldrich
Beschreibung:
(S)-(+)-1-Aminoindan, Sigma-Aldrich®
Artikel-Nr:
(MOLEM36908126)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M36908126
Lokale Artikelnummer::
MOLEM36908126
Beschreibung:
5-Aminochinolin
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-4176R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-A488
Lokale Artikelnummer::
BOSSBS-4176R-A488
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-FITC
Lokale Artikelnummer::
BOSSBS-4176R-FITC
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-A350
Lokale Artikelnummer::
BOSSBS-4176R-A350
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL193232-10G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
193232-10G
Lokale Artikelnummer::
SIAL193232-10G
Beschreibung:
6-Amino-1,4-benzodioxan, Sigma-Aldrich®
VE:
1 * 10 g
Lieferant:
Sigma-Aldrich
Beschreibung:
1-Aminobenzotriazol, Sigma-Aldrich®
Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-4-phenylthiazol
Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-4-methylpyridin
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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