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Artikel-Nr:
(BOSSBS-11075R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11075R
Lokale Artikelnummer::
BOSSBS-11075R
Beschreibung:
CNTNAP3B is a 1,288 amino acid protein that is encoded by a gene which maps to human chromosome 9. Chromosome 9 contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10348R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10348R
Lokale Artikelnummer::
BOSSBS-10348R
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(SIAL684686-250MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
684686-250MG
Lokale Artikelnummer::
SIAL684686-250MG
Beschreibung:
2,2-Difluorpropionsäure, Sigma-Aldrich®
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-8870R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8870R-CY7
Lokale Artikelnummer::
BOSSBS-8870R-CY7
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Lieferant:
VWR Chemicals
Beschreibung:
Alizarinrot S (Natriumsalz), AnalaR NORMAPUR® Reag. Ph. Eur. analytisches Reagens (C.I. 58005)
Lieferant:
Merck
Beschreibung:
EDTA Dikaliumsalz Dihydrat zur Synthese, Sigma-Aldrich®
Lieferant:
FLUOROCHEM
Beschreibung:
2,2-Difluorpropionsäure
Lieferant:
Thermo Scientific
Beschreibung:
Alizarinrot S (Natriumsalz), rein, zertifiziert
Artikel-Nr:
(EHERC17486500)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C17486500
Lokale Artikelnummer::
EHERC17486500
Beschreibung:
2,2'-Thiodiessigsäure
VE:
1 * 0,25 g
Artikel-Nr:
(BOSSBS-10348R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10348R-A647
Lokale Artikelnummer::
BOSSBS-10348R-A647
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10348R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10348R-FITC
Lokale Artikelnummer::
BOSSBS-10348R-FITC
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11914R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11914R-CY3
Lokale Artikelnummer::
BOSSBS-11914R-CY3
Beschreibung:
Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(FLUO024173-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
024173-1G
Lokale Artikelnummer::
FLUO024173-1G
Beschreibung:
2,2-Difluorcyclopropancarbonsäure
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11914R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11914R-A555
Lokale Artikelnummer::
BOSSBS-11914R-A555
Beschreibung:
Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13441R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13441R-CY5
Lokale Artikelnummer::
BOSSBS-13441R-CY5
Beschreibung:
Glutathione (GSH) is a tripeptide antioxidant which reduces disulfide bonds between cytoplasmic proteins. The constitutive enzyme glutathione reductase transforms glutathione into its reduced state which ultimately can provide a measure of cellular toxicity. GSTT2 (glutathione S-transferase theta-2), also known as GST class-theta-2, is a 244 amino acid enzyme with sulfatase activity that functions in conjugating reduced glutathione to hydrophobic electrophiles. GSTT2 exists as a homodimer in the cytoplasm and is expressed in low levels in the liver and the lung. GSTT2 belongs to the GST superfamily and contains both a GST C-terminal and a GST N-terminal domain. The gene encoding GSTT2 exists on human chromosome 22.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8870R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8870R-A488
Lokale Artikelnummer::
BOSSBS-8870R-A488
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
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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