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6,7-Dimethylchinolin-2,3-dicarbons\u00E4ure


30 019  results were found

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Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-3769R-A680
Lokale Artikelnummer:: BOSSBS-3769R-A680
Beschreibung:   Modulation of the chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of four core histone proteins (H2A, H2B, H3 and H4), is the primary building block of chromatin. The N-terminal tail of core histones undergoes different posttranslational modifications including acetylation, phosphorylation and methylation. These modifications occur in response to cell signal stimuli and have a direct effect on gene expression. In most species, the histone H2B is primarily acetylated at lysines 5, 12, 15 and 20. Histone H3 is primarily acetylated at lysines 9, 14, 18 and 23. Acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms. Phosphorylation at Ser10 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis.
VE:  1 * 100 µl
Artikel-Nr: (SIALN17807-5G)

Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: N17807-5G
Lokale Artikelnummer:: SIALN17807-5G
Beschreibung:   5-Nitroisatin, Sigma-Aldrich®
VE:  1 * 5 g
Artikel-Nr: (EHERCA13175000)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: CA13175000
Lokale Artikelnummer:: EHERCA13175000
Beschreibung:   (±)-Epichlorhydrin
VE:  1 * 1 mL
Artikel-Nr: (FLUO018460-10G)

Lieferant:  FLUOROCHEM
Hersteller-Artikelnummer:: 018460-10G
Lokale Artikelnummer:: FLUO018460-10G
Beschreibung:   3-Chlor-o-xylol
VE:  1 * 10 g
Market Source Item This is a MarketSource item. Additional charges may apply
Artikel-Nr: (BOSSBS-12498R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12498R-CY5
Lokale Artikelnummer:: BOSSBS-12498R-CY5
Beschreibung:   Apolipoproteins are protein components of plasma lipoproteins (1). The apolipoprotein L gene family encodes six highly homologous proteins designated apoL-I to -VI, which are associated with large high density type lipoproteins (HDL) (2,3). The human apoL family maps to chromosome 22q12.1-13.1 within a 127,000-bp region (4). ApoL has been characterized as a pancreas specific, 383-amino acid protein that contains a 12-amino acid secretory signal peptide (4). The apoL genes have TATA-less promoters and contain putative sterol regulatory elements, suggesting that transcription of these genes may be coordinated with that of the low density lipoprotein receptor and genes in pathways involving the synthesis of triglycerides and cholesterol (3). ApoL homologs can undergo 10 fold changes in expression during atherosclerotic changes in vascular endothelial cells, which includes the inflammatory reaction of atherosclerotic lesions (5).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-12498R-CY7)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12498R-CY7
Lokale Artikelnummer:: BOSSBS-12498R-CY7
Beschreibung:   Apolipoproteins are protein components of plasma lipoproteins (1). The apolipoprotein L gene family encodes six highly homologous proteins designated apoL-I to -VI, which are associated with large high density type lipoproteins (HDL) (2,3). The human apoL family maps to chromosome 22q12.1-13.1 within a 127,000-bp region (4). ApoL has been characterized as a pancreas specific, 383-amino acid protein that contains a 12-amino acid secretory signal peptide (4). The apoL genes have TATA-less promoters and contain putative sterol regulatory elements, suggesting that transcription of these genes may be coordinated with that of the low density lipoprotein receptor and genes in pathways involving the synthesis of triglycerides and cholesterol (3). ApoL homologs can undergo 10 fold changes in expression during atherosclerotic changes in vascular endothelial cells, which includes the inflammatory reaction of atherosclerotic lesions (5).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15323R-HRP)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15323R-HRP
Lokale Artikelnummer:: BOSSBS-15323R-HRP
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

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15323R-A555
Lokale Artikelnummer:: BOSSBS-15323R-A555
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
Lieferant:  COMBI-BLOCKS
Beschreibung:   7-Fluorisatin
Lieferant:  Thermo Scientific
Beschreibung:   5-Bromisatin
Artikel-Nr: (MENASR462.10)

Lieferant:  MENAI
Hersteller-Artikelnummer:: SR462.10
Lokale Artikelnummer:: MENASR462.10
Beschreibung:   4,7-Dichlorisatin
VE:  1 * 10 g
Lieferant:  WITEG LABORTECHNIK
Beschreibung:   Borosilicate glass 3.3.
Lieferant:  BIOLEGEND INC
Beschreibung:   Anti-VDAC1 Mouse Monoclonal Antibody [clone: N152B/23]

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12498R-A488
Lokale Artikelnummer:: BOSSBS-12498R-A488
Beschreibung:   Apolipoproteins are protein components of plasma lipoproteins (1). The apolipoprotein L gene family encodes six highly homologous proteins designated apoL-I to -VI, which are associated with large high density type lipoproteins (HDL) (2,3). The human apoL family maps to chromosome 22q12.1-13.1 within a 127,000-bp region (4). ApoL has been characterized as a pancreas specific, 383-amino acid protein that contains a 12-amino acid secretory signal peptide (4). The apoL genes have TATA-less promoters and contain putative sterol regulatory elements, suggesting that transcription of these genes may be coordinated with that of the low density lipoprotein receptor and genes in pathways involving the synthesis of triglycerides and cholesterol (3). ApoL homologs can undergo 10 fold changes in expression during atherosclerotic changes in vascular endothelial cells, which includes the inflammatory reaction of atherosclerotic lesions (5).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15323R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15323R-CY3
Lokale Artikelnummer:: BOSSBS-15323R-CY3
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
Lieferant:  COMBI-BLOCKS
Beschreibung:   5-Fluorisatin
Preis auf Anfrage
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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