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1-(3-Methoxyphenyl)cyclopropanecarboxylic+acid
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1-(3-Methoxyphenyl)cyclopropanecarboxylic+acid
Artikel-Nr:
(BLDPBD46863-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD46863-10G
Lokale Artikelnummer::
BLDPBD46863-10G
Beschreibung:
(R)-(-)-2,2-Dimethyl-1,3-dioxolan-4-ylmethyl-p-toluenesulphonate 97%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-3730R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3730R-CY5.5
Lokale Artikelnummer::
BOSSBS-3730R-CY5.5
Beschreibung:
Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. There have been at least 12 different PKC isoforms identified in humans to date including alpha, beta I, beta II, gamma, delta, epsilon, zeta, eta, theta, iota, lambda, and mu. PKC gamma is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3626R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3626R-CY5.5
Lokale Artikelnummer::
BOSSBS-3626R-CY5.5
Beschreibung:
Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. There have been at least 12 different PKC isoforms identified in humans to date including alpha, beta I, beta II, gamma, delta, epsilon, zeta, eta, theta, iota, lambda, and mu. PKC gamma is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10161R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10161R-A555
Lokale Artikelnummer::
BOSSBS-10161R-A555
Beschreibung:
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10161R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10161R-FITC
Lokale Artikelnummer::
BOSSBS-10161R-FITC
Beschreibung:
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD1586-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD1586-500G
Lokale Artikelnummer::
BLDPBD1586-500G
Beschreibung:
(2R)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutansäure 98%
VE:
1 * 500 g
Artikel-Nr:
(BLDPBD0230-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD0230-1G
Lokale Artikelnummer::
BLDPBD0230-1G
Beschreibung:
2-Methyl-2-propanyl-3-cyan-4-oxo-1-pyrrolidincarboxylat 97%
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD239499-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD239499-250MG
Lokale Artikelnummer::
BLDPBD239499-250MG
Beschreibung:
5-(Hydroxymethyl)-3-methylisoxazole 97%
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-11571R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11571R
Lokale Artikelnummer::
BOSSBS-11571R
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic Alpha/Beta horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. The LRRTM protein family plays a role in the regulation of various cellular events during nervous system development. Localizing predominantly to the nervous system, LRRTM family members are known to exhibit synaptogenic activity. LRRTM3 (leucine rich repeat transmembrane neuronal 3) is a 581 amino acid single-pass type I membrane protein belonging to the LRRTM family. LRRTM3 is involved in the development and maintenance of the vertebrate nervous system, and contains ten LRR repeats. Expressed in neuronal tissues, LRRTM3 is encoded by a gene that maps to a region of chromosome 10 that has been linked to late-onset Alzheimer disease and elevated plasma Beta-Amyloid. As a result of alternative splicing events, two LRRTM3 isoforms exist.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10161R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10161R-CY3
Lokale Artikelnummer::
BOSSBS-10161R-CY3
Beschreibung:
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
N-Methyl-4-boronobenzolsulfonamid pinacol ester
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-Methylethylendiamin 95%
Lieferant:
Sigma-Aldrich
Beschreibung:
o-Terphenyl, Sigma-Aldrich®
Artikel-Nr:
(BLDPBD122324-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD122324-1G
Lokale Artikelnummer::
BLDPBD122324-1G
Beschreibung:
7-(Diethylamino)-3-(1-methyl-2-benzimidazolyl)coumarin 98%
VE:
1 * 1 g
Artikel-Nr:
(ACRO456250010)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
456250010
Lokale Artikelnummer::
ACRO456250010
Beschreibung:
Paliperidone 98%
VE:
1 * 1 g
Lieferant:
Thermo Scientific
Beschreibung:
2-Undecanon 98%
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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