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Proteine und Peptide
Artikel-Nr:
(BOSSBS-11822R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-CY3
Lokale Artikelnummer::
BOSSBS-11822R-CY3
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-11698R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A555
Lokale Artikelnummer::
BOSSBS-11698R-A555
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-11698R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A680
Lokale Artikelnummer::
BOSSBS-11698R-A680
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 1100 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-11698R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-FITC
Lokale Artikelnummer::
BOSSBS-11698R-FITC
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2',3'-Difluoracetophenon 98%
Lieferant:
Alfa Aesar
Beschreibung:
3',5'-Dimethoxyacetophenon ≥97%
Lieferant:
Alfa Aesar
Beschreibung:
Boc-trans-4-amino-L-proline methyl ester hydrochloride salt 97%
Lieferant:
Alfa Aesar
Beschreibung:
4-Bromphenylisothiocyanat ≥97%
Artikel-Nr:
(BLDPBD301409-25MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD301409-25MG
Lokale Artikelnummer::
BLDPBD301409-25MG
Beschreibung:
5-Bromo-1,3-dihydrobenzo[c]thiophene 2,2-dioxide 97%
VE:
1 * 25 mg
Artikel-Nr:
(BLDPBD73092-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD73092-10G
Lokale Artikelnummer::
BLDPBD73092-10G
Beschreibung:
2-Chloro-5-(methylthio)benzoic acid 97%
VE:
1 * 10 g
Artikel-Nr:
(BNUM0810-50)
Lieferant:
Biotium
Hersteller-Artikelnummer::
BNUM0810-50
Lokale Artikelnummer::
BTIUBNUM0810-50
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.
VE:
1 * 50 µl
Artikel-Nr:
(APOSOR32618-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR32618-1G
Lokale Artikelnummer::
APOSOR32618-1G
Beschreibung:
(2-Methyl-3-phenyltetrahydro-5-isoxazolyl)methanol 95%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,3-Dimethylphenylisocyanat 97%
Artikel-Nr:
(APOSPC0259-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC0259-1G
Lokale Artikelnummer::
APOSPC0259-1G
Beschreibung:
2,3-Difluor-p-kresol
VE:
1 * 1 g
Artikel-Nr:
(APOSOR52273-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR52273-1G
Lokale Artikelnummer::
APOSOR52273-1G
Beschreibung:
tert-Butyl 2-(piperidin-4-yl)pyrrolidine-1-carboxylate
VE:
1 * 1 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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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