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(R)-Methyl+4,4-difluoropyrrolidine-2-carboxylate+hydrochloride
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(R)-Methyl+4,4-difluoropyrrolidine-2-carboxylate+hydrochloride
Artikel-Nr:
(BOSSBS-11229R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11229R-A680
Lokale Artikelnummer::
BOSSBS-11229R-A680
Beschreibung:
OTUB1 is a 271 amino acid protein that contains one OTU (ovarian tumour) domain and belongs to the OTU family of predicted cysteine proteases. Expressed as two isoforms (one of which is present throughout the body and the other of which is present only in lymphoid tissues), OTUB1 functions as a hydrolase that can remove ubiquitin residues from target proteins, thereby preventing protein degradation and playing an important role in protein turnover. OTUB1 interacts with GRAIL and, via this interaction, plays a role in the regulation and the induction of T-cell anergy, a phenomenon that occurs when T-cells are rendered unresponsive to their cognate antigens. Due to its interaction with GRAIL, OTUB1 is an important regulator of immune responses in secondary lymphoid organs.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13573R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13573R-HRP
Lokale Artikelnummer::
BOSSBS-13573R-HRP
Beschreibung:
ZBTB39 may be involved in transcriptional regulation. It belongs to the krueppel C2H2-type zinc-finger protein family and contains one BTB (POZ) domain and eight C2H2-type zinc fingers.
VE:
1 * 100 µl
Lieferant:
Hichrom Limited
Beschreibung:
Vydac TP ist die erste im Vydac-Sortiment entwickelte Reihe weitporiger Medienphasen und ist der Branchenstandard für Peptid- und Proteintrennungen. Die großen Poren des 300-Å-TP-Silica ermöglichen Polypeptidmolekülen vollständigen Zugang zum Inneren der Silica-Poren.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 6-aminopyrimidine-4-carboxylate 95%
Artikel-Nr:
(BOSSBS-11822R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A680
Lokale Artikelnummer::
BOSSBS-11822R-A680
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyses 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-8229R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-FITC
Lokale Artikelnummer::
BOSSBS-8229R-FITC
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9950R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9950R-A680
Lokale Artikelnummer::
BOSSBS-9950R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The C12orf50 gene product has been provisionally designated C12orf50 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A750
Lokale Artikelnummer::
BOSSBS-11945R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9944R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9944R-A750
Lokale Artikelnummer::
BOSSBS-9944R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The C12orf4 gene product has been provisionally designated C12orf4 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9944R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9944R-A680
Lokale Artikelnummer::
BOSSBS-9944R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The C12orf4 gene product has been provisionally designated C12orf4 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A488
Lokale Artikelnummer::
BOSSBS-8229R-A488
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 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. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. 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. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0424R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0424R-CY5.5
Lokale Artikelnummer::
BOSSBS-0424R-CY5.5
Beschreibung:
Cleaves collagens of types I, II, and III at one site in the helical domain. Also cleaves collagens of types VII and X. In case of HIV infection, interacts and cleaves the secreted viral Tat protein, leading to a decrease in neuronal Tat's mediated neurotoxicity.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD2942-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD2942-1G
Lokale Artikelnummer::
BLDPBD2942-1G
Beschreibung:
Methyl-3-(methylamino)but-2-enoate 97%
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD00858192-250)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD00858192-250
Lokale Artikelnummer::
BLDPBD00858192-250
Beschreibung:
2-(5-BROMO-2-FLUOROPHENYL)PYRROLIDINE HCL 95%
VE:
1 * 250 mg
Artikel-Nr:
(SCOI285403786)
Lieferant:
SI Analytics
Hersteller-Artikelnummer::
285403786
Lokale Artikelnummer::
SCOI285403786
Beschreibung:
Cannon-Fenske viscometers for automatic measurements especially in routine analyses.
VE:
1 * 1 ST
Lieferant:
Molecular Devices
Beschreibung:
The Neurotransmitter Transporter Uptake Assay Kit provides a fast, simple and reliable fluorescence-based assay for the detection of dopamine, norepinephrine and serotonin transporter (SERT, NET and DAT, respectively) activity in expressing cells.
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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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