Methylpyrazolo[1,5-a]pyridin-3-carboxylat
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-(Trifluormethyl)-5-pyridinboronsäure
Artikel-Nr:
(BOSSBS-7921R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-A350
Lokale Artikelnummer::
BOSSBS-7921R-A350
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Lieferant:
EDQM
Beschreibung:
Organic Standard, Imatinib impurity H, 1-(pyridin-3-yl)ethan-1-one, Ph. Eur. standard
Artikel-Nr:
(BOSSBS-4148R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4148R-CY3
Lokale Artikelnummer::
BOSSBS-4148R-CY3
Beschreibung:
PKMYT1 is a member of the serine/threonine protein kinase family. It preferentially phosphorylates and inactivates cell division cycle 2 protein (cdc2), and thus acts as a negative regulator of entry into mitosis (G2 to M transition). It mediates phosphorylation of cdc2 predominantly on 'Thr-14' and is also involved in Golgi fragmentation. It may be involved in phosphorylation of cdc2 on 'Tyr-15' to a lesser degree, however tyrosine kinase activity is unclear and may be indirect. It may be a downstream target of Notch signaling pathway during eye development. PKMYT1 is negatively regulated by hyperphosphorylation during mitosis.
VE:
1 * 100 µl
Lieferant:
Restek
Beschreibung:
Organic Standard, Pyridine, 2000 µg/ml, purge and trap grade methanol, 1 ml/ampule
Lieferant:
Sigma-Aldrich
Beschreibung:
Bis(1,5-cyclooctadien)rhodium(I)hexafluoroantimonat, Sigma-Aldrich®
Lieferant:
WTW
Beschreibung:
Qualitätsgeräte mit erweiterter Messtechnik und neuen Funktionen wie automatischer AutoRead-Funktion, CMC (Continuous Measurement Control, Kontinuierliche Messwertkontrolle) und QSC (Quality Sensor Control, Sensorzustandskontrolle), mit denen Messungen bequemer und zuverlässiger als jemals zuvor durchgeführt werden können.
Artikel-Nr:
(SIAL125857-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
125857-5G
Lokale Artikelnummer::
SIAL125857-5G
Beschreibung:
2,3-Diaminopyridin, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(MOLE28391632-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
28391632-100G
Lokale Artikelnummer::
MOLE28391632-100G
Beschreibung:
2,5-Pyridindicarbonsäure
VE:
1 * 100 g
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Artikel-Nr:
(MOLEM11577982)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M11577982
Lokale Artikelnummer::
MOLEM11577982
Beschreibung:
2,5-Pyridindicarbonsäure
VE:
1 * 500 g
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Artikel-Nr:
(BOSSBS-3818R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3818R-FITC
Lokale Artikelnummer::
BOSSBS-3818R-FITC
Beschreibung:
Growth differentiation factor 15 (GDF15) is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. It has been implicated in a variety of functions directly related to tumorigenicity including antiproliferative and pro-apoptotic effects. BMP proteins are secreted growth factors that are characterized by seven conserved cysteine residues. In general, they are regulators of cell growth and differentiation in both embryonic and adult tissues.GDF15 is an important downstream mediator of DNA damage signaling and a transcriptional target of p53.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9976R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9976R-A750
Lokale Artikelnummer::
BOSSBS-9976R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf128 gene product has been provisionally designated C21orf128 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9975R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9975R-A680
Lokale Artikelnummer::
BOSSBS-9975R-A680
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-FITC
Lokale Artikelnummer::
BOSSBS-15130R-FITC
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-A488
Lokale Artikelnummer::
BOSSBS-15130R-A488
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
1,5-Bis(diphenylphosphino)pentan, Sigma-Aldrich®
Preis auf Anfrage
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