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2,2\'-Bipyridin-4,4\'-dicarbonsäure
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2,2\'-Bipyridin-4,4\'-dicarbonsäure
Artikel-Nr:
(BOSSBS-11822R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A350
Lokale Artikelnummer::
BOSSBS-11822R-A350
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
N-(3-Brompropyl)phthalimid 98%
Artikel-Nr:
(SIAL803219-50MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
803219-50MG
Lokale Artikelnummer::
SIAL803219-50MG
Beschreibung:
EGS is a water-insoluble, homobifunctional N-hydroxysuccinimide ester (NHS ester) and Sulfo-EGS is its water-soluble analog. The spacer arm contains two cleavable ester sites that may be broken with hydroxylamine, which yields two fragments with terminal amide bonds and the release of ethylene glycol. These reagents are often used for conjugating radiolabeled ligands to cell surface receptors. The water insoluble reagent EGS does not possess a charged group, is lipophilic and, therefore, membrane-permeable and useful for intracellular and intramembrane protein conjugation. EGS is first dissolved in DMSO or DMF and added to the aqueous reaction mixture at a final solvent concentration of 10-20%, to minimize detrimental affects to the protein.
VE:
1 * 50 mg
Artikel-Nr:
(BOSSBS-8130R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-CY5.5
Lokale Artikelnummer::
BOSSBS-8130R-CY5.5
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8130R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-FITC
Lokale Artikelnummer::
BOSSBS-8130R-FITC
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
VWR Collection
Beschreibung:
Heizbad für LED-Rotationsverdampfer, Raumtemperatur bis 180 °C, VWR®, Für: LED-Rotationsverdampfer
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 2-(1H-pyrazol-1-yl)acetate 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
[3-Phenyl-5-isoxazolyl]methanol 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Methoxy-5-methylbenzotrifluoride 95%
Artikel-Nr:
(BOSSBS-12345R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY3
Lokale Artikelnummer::
BOSSBS-12345R-CY3
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY5
Lokale Artikelnummer::
BOSSBS-12345R-CY5
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
Pall Laboratory
Beschreibung:
Ideal zur Probenpräparation und für Detektionsverfahren mit hohem Durchsatz. Die AcroPrep™ Filterplatten sind aus chemisch beständigem, biologisch inertem PP gefertigt, besitzen einen transparenten Deckel aus PS und sind in einer Vielzahl von Membrankonfigurationen verfügbar, um den Anforderungen verschiedener Anwendungen gerecht zu werden.
Artikel-Nr:
(BOSSBS-5049R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-A488
Lokale Artikelnummer::
BOSSBS-5049R-A488
Beschreibung:
Catalyzes the first step in the oxidation of the side chain of sterol intermediates; the 27-hydroxylation of 5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol. Has also a vitamin D3-25-hydroxylase activity.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
This antibody recognizes an oncofetal glycoprotein with a single chain of 70 kDa, which is identified as alpha fetoprotein (AFP). This MAb is highly specific to AFP and shows no cross-reaction with other oncofetal antigens or serum albumin. AFP is normally synthesized in the liver, intestinal tract, and yolk sac of the fetus. Antibody to AFP has been shown to be useful in detecting hepatocellular carcinomas (HCC) and germ cell neoplasms, especially yolk sac tumors.
Artikel-Nr:
(BOSSBS-12946R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12946R
Lokale Artikelnummer::
BOSSBS-12946R
Beschreibung:
CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12163R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12163R
Lokale Artikelnummer::
BOSSBS-12163R
Beschreibung:
CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
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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