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1,6-Anhydro-\\u03B2-D-mannopyranose
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1,6-Anhydro-\\u03B2-D-mannopyranose
Artikel-Nr:
(BOSSBS-12039R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-HRP
Lokale Artikelnummer::
BOSSBS-12039R-HRP
Beschreibung:
GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
2-Nitrobenzoesäure 95%
Artikel-Nr:
(BOSSBS-1610R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1610R-A647
Lokale Artikelnummer::
BOSSBS-1610R-A647
Beschreibung:
Blocks interferon-dependent interphase and stimulates DNA synthesis in cells. Involved in the translational regulation of the human papillomavirus type 16 E7 mRNA (HPV16 E7).
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR24839-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR24839-250MG
Lokale Artikelnummer::
APOSOR24839-250MG
Beschreibung:
N-Benzyl-N-(2-chloroethyl)amine 90+%
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-13752R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13752R-CY7
Lokale Artikelnummer::
BOSSBS-13752R-CY7
Beschreibung:
Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Involved in paracellular magnesium reabsorption. Required for a selective paracellular conductance. May form, alone or in partnership with other constituents, an intercellular pore permitting paracellular passage of magnesium and calcium ions down their electrochemical gradients. Alternatively, it could be a sensor of magnesium concentration that could alter paracellular permeability mediated by other factors.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD517781-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD517781-100G
Lokale Artikelnummer::
BLDPBD517781-100G
Beschreibung:
Dimethyl 5-methylpyridine-2,3-dicarboxylate 97%
VE:
1 * 100 g
Lieferant:
Sartorius Balances
Beschreibung:
Sartorius Proof Line weights are high quality working standards for everyday use. These weights are made of high quality material with polished or precision lathed surfaces.
Artikel-Nr:
(BOSSBS-7987R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7987R-CY7
Lokale Artikelnummer::
BOSSBS-7987R-CY7
Beschreibung:
This gene encodes for a coiled coil domain containing 16 protein and is located on chromosome 17. The protein may act as a regulator of the cell cycle in embryos by participating in control of M phase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8320R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8320R-HRP
Lokale Artikelnummer::
BOSSBS-8320R-HRP
Beschreibung:
HEATR3 is a 680 amino acid protein existing as three alternatively spliced isoforms and containing two HEAT (Huntingtin, elongation factor 3 (EF3), protein phosphatase 2A (PP2A) and the yeast PI3-kinase Tor1) repeats. HEAT repeats form rod-like helical structures that are involved in intracellular transport. HEATR3 is encoded by a gene located on human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8320R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8320R-FITC
Lokale Artikelnummer::
BOSSBS-8320R-FITC
Beschreibung:
HEATR3 is a 680 amino acid protein existing as three alternatively spliced isoforms and containing two HEAT (Huntingtin, elongation factor 3 (EF3), protein phosphatase 2A (PP2A) and the yeast PI3-kinase Tor1) repeats. HEAT repeats form rod-like helical structures that are involved in intracellular transport. HEATR3 is encoded by a gene located on human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8320R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8320R-A680
Lokale Artikelnummer::
BOSSBS-8320R-A680
Beschreibung:
HEATR3 is a 680 amino acid protein existing as three alternatively spliced isoforms and containing two HEAT (Huntingtin, elongation factor 3 (EF3), protein phosphatase 2A (PP2A) and the yeast PI3-kinase Tor1) repeats. HEAT repeats form rod-like helical structures that are involved in intracellular transport. HEATR3 is encoded by a gene located on human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
DURAN®, borosilicate glass.
Artikel-Nr:
(BOSSBS-8414R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8414R-FITC
Lokale Artikelnummer::
BOSSBS-8414R-FITC
Beschreibung:
The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8414R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8414R-CY5
Lokale Artikelnummer::
BOSSBS-8414R-CY5
Beschreibung:
The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
VE:
1 * 100 µl
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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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