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N1-Methylbenzene-1,2-diamine+dihydrochloride
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N1-Methylbenzene-1,2-diamine+dihydrochloride
Lieferant:
Alfa Aesar
Beschreibung:
5,5-Dimethyl-1,3-dioxan-2-one, tech.
Artikel-Nr:
(B20921.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
B20921.06
Lokale Artikelnummer::
ALFAB20921.06
Beschreibung:
5-(2,3-Dichlorphenyl)-1H-tetrazol 97
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-11822R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-FITC
Lokale Artikelnummer::
BOSSBS-11822R-FITC
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
Artikel-Nr:
(BOSSBS-11822R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-HRP
Lokale Artikelnummer::
BOSSBS-11822R-HRP
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
Artikel-Nr:
(BOSSBS-8130R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-A680
Lokale Artikelnummer::
BOSSBS-8130R-A680
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:
(BLDPBD01123462-100)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01123462-100
Lokale Artikelnummer::
BLDPBD01123462-100
Beschreibung:
Ethyl 4-chloro-5-(trifluoromethyl)quinoline-3-carboxylate 98%
VE:
1 * 100 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Acetyl-3-amino-5-(4-tert-butylphenyl)thiophene 97%
Artikel-Nr:
(BOSSBS-12345R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY7
Lokale Artikelnummer::
BOSSBS-12345R-CY7
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:
(T265-01)
Lieferant:
Avantor
Lokale Artikelnummer::
BAKRT265-01
Beschreibung:
Powder. Lot analysis on label.
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-tert-Butyl-4-methyl-1H-indole 95+%
Artikel-Nr:
(BOSSBS-12946R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12946R-CY7
Lokale Artikelnummer::
BOSSBS-12946R-CY7
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-0019R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0019R-CY3
Lokale Artikelnummer::
BOSSBS-0019R-CY3
Beschreibung:
Acts as a cytokine involved in enhancing production of interferon-gamma and interleukin-12 and reducing production of interleukin-10 and is essential in the pathway that leads to type I immunity (By similarity).
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Appearance: Colorless to white Crystalline powder or crystals
Artikel-Nr:
(BOSSBS-11698R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-CY5
Lokale Artikelnummer::
BOSSBS-11698R-CY5
Beschreibung:
Huntingtin yeast partner E is a 458 amino acid single-pass membrane protein. HYPE is thought to interact with Huntingtin, a protein which induces neurodegeneration when mutated. HYPE also contains two tetratricopeptide repeats (TPR), which may be involved in protein-protein interaction. The gene that encodes HYPE is located on chromosome 12, which encodes over 1,100 genes within 132 million bases and makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3842R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-CY5
Lokale Artikelnummer::
BOSSBS-3842R-CY5
Beschreibung:
EIF3S3 binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA. It associates with the p170 subunit of EIF3. The EIF3 is composed of at least 12 different subunits.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD63453-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD63453-100G
Lokale Artikelnummer::
BLDPBD63453-100G
Beschreibung:
2-Hydroxyethyl-phenylsulfid 97%
VE:
1 * 100 g
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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