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Boc-(S)-thiazolidine-2-carboxylic+acid
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Boc-(S)-thiazolidine-2-carboxylic+acid
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
Artikel-Nr:
(EHERC12723300)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C12723300
Lokale Artikelnummer::
EHERC12723300
Beschreibung:
4-(Dimethylamino)pyridin
VE:
1 * 0,1 g
Artikel-Nr:
(SIAL38497-100ML-F)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
38497-100ML-F
Lokale Artikelnummer::
SIAL38497-100ML-F
Beschreibung:
1-Naphthylamin, Millipore®
VE:
1 * 100 mL
Lieferant:
Novabiochem (Part of Merck)
Beschreibung:
4-(Dimethylamino)pyridin
Artikel-Nr:
(MAYBSB01321.50)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
SB01321.50
Lokale Artikelnummer::
MAYBSB01321.50
Beschreibung:
4-Aminopyridin
VE:
1 * 50 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Thermo Scientific
Beschreibung:
3-Amino-4-brom-5-methylisoxazol
Lieferant:
Thermo Scientific
Beschreibung:
The amine group is the most common target for modifying protein molecules because it is abundant in the majority of proteins either due to the presence of lysine bearing amino side chain functionality or the N-terminal-amine. Amine-reactive biotinylation reagents can be divided into two groups based on water solubility: NHS-esters and sulfo-NHS-esters.
Artikel-Nr:
(MOLE17295435-5G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
17295435-5G
Lokale Artikelnummer::
MOLE17295435-5G
Beschreibung:
8-Aminochinolin
VE:
1 * 5 g
This is a MarketSource item. Additional charges may apply
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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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