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3-Aminopiperidine+hydrochloride,+N1-CBZ+protected
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3-Aminopiperidine+hydrochloride,+N1-CBZ+protected
Lieferant:
Biotium
Beschreibung:
This MAb recognizes a 22 kDa protein, identified as Transgelin, also designated SM22-alpha. It may cross-react with SM22-beta. Transgelin is expressed abundantly in smooth muscle cells. The human transgelin gene encodes a 201 amino acid protein that contains nuclear factor-binding motifs known to regulate transcription in smooth muscle. During embryogenesis, transgelin is expressed in smooth, cardiac and skeletal muscle, but is restricted during late fetal development and adulthood to all vascular and visceral smooth muscle cells and low levels of expression in heart. Transgelin is down regulated in several transformed cell lines, indicating that a reduction of transgelin expression may be an early indicator of the onset of transformation. Transgelin also binds Actin, causing Actin fibers to gel within minutes of binding. Binding of transgelin to Actin occurs at a ratio of 1:6 Actin monomers.
Artikel-Nr:
(BOSSBS-9495R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9495R-CY5
Lokale Artikelnummer::
BOSSBS-9495R-CY5
Beschreibung:
C9orf117 is a 520 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf117 maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15323R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15323R-CY7
Lokale Artikelnummer::
BOSSBS-15323R-CY7
Beschreibung:
C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9498R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9498R-A555
Lokale Artikelnummer::
BOSSBS-9498R-A555
Beschreibung:
C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15316R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15316R-CY5
Lokale Artikelnummer::
BOSSBS-15316R-CY5
Beschreibung:
C9orf16 (chromosome 9 open reading frame 16) is an 83 amino acid protein that belongs to the UPF0184 (EST00098) family and is encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15321R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15321R-HRP
Lokale Artikelnummer::
BOSSBS-15321R-HRP
Beschreibung:
C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Lieferant:
Bernd Kraft
Beschreibung:
Natriumacetat 30% in wässriger Lösung, reinst
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-(Carboxymethyl)phenylboronsäure
Lieferant:
Thermo Scientific
Beschreibung:
Natriumacetat Trihydrat 99.5% zur Analyse
Artikel-Nr:
(APPC141211.1211)
Lieferant:
APPLICHEM
Hersteller-Artikelnummer::
141211.1211
Lokale Artikelnummer::
APPC141211.1211
Beschreibung:
Calciumacetat 99,0-100,5% USP
VE:
1 * 1.000 g
Lieferant:
Bernd Kraft
Beschreibung:
Magnesiumacetat Tetrahydrat, reinst
Artikel-Nr:
(MOLE10722816-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
10722816-100G
Lokale Artikelnummer::
MOLE10722816-100G
Beschreibung:
4-Aminohippursäure
VE:
1 * 100 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Bernd Kraft
Beschreibung:
Natriumacetat 0.5 mol/l (0.5 N) in wässriger Lösung
Lieferant:
Bernd Kraft
Beschreibung:
Cadmiumacetat 5%, reinst
Lieferant:
LONZA
Beschreibung:
EDTA Dinatriumsalz-Lösung 0.5 M, AccuGENE®
Artikel-Nr:
(SIAL333301-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
333301-5G
Lokale Artikelnummer::
SIAL333301-5G
Beschreibung:
2-Methyl-3-indolylessigsäure, Sigma-Aldrich®
VE:
1 * 5 g
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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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