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Lieferant:
EDQM
Beschreibung:
Organic Standard, Imatinib impurity H, 1-(pyridin-3-yl)ethan-1-one, Ph. Eur. standard
Artikel-Nr:
(MOLEM11947640)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M11947640
Lokale Artikelnummer::
MOLEM11947640
Beschreibung:
7-Azaindol
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
Nicotinamid, Sigma-Aldrich®
Artikel-Nr:
(FLUO136900-25G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
136900-25G
Lokale Artikelnummer::
FLUO136900-25G
Beschreibung:
2,2'-Dipyridyldisulfid
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
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
Artikel-Nr:
(BOSSBS-10410R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10410R-CY5
Lokale Artikelnummer::
BOSSBS-10410R-CY5
Beschreibung:
Chemerin, also known as retinoic acid receptor responder 2 (RARRES2) and tazarotene induced gene 2 (TIG2), is a chemoattractant protein for cells expressing G-protein-linked receptor chemokine-like receptor 1 (CMKLR1, ChemR23 or GPCR-DEZ). The protein is synthesized as a secreted precursor, prochemerin (18 kDa), which is poorly active. Upon proteolytic removal of the last six amino acids, prochemerin is converted into mature active chemerin (15-16 kDa) that acts as a strong and highly specific agonist of its receptor CMKLR1. Chemerin is a newly described adipokine with effects on adipocyte differnetiation and metabolism.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3814R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3814R-A680
Lokale Artikelnummer::
BOSSBS-3814R-A680
Beschreibung:
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E1 ubiquitin-activating enzyme family. The encoded enzyme is a retinoid target that triggers promyelocytic leukaemia (PML)/retinoic acid receptor alpha (RARalpha) degradation and apoptosis in acute promyelocytic leukaemia, where it is involved in the conjugation of the ubiquitin-like interferon-stimulated gene 15 protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3814R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3814R-A750
Lokale Artikelnummer::
BOSSBS-3814R-A750
Beschreibung:
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E1 ubiquitin-activating enzyme family. The encoded enzyme is a retinoid target that triggers promyelocytic leukaemia (PML)/retinoic acid receptor alpha (RARalpha) degradation and apoptosis in acute promyelocytic leukaemia, where it is involved in the conjugation of the ubiquitin-like interferon-stimulated gene 15 protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-CY3
Lokale Artikelnummer::
BOSSBS-15130R-CY3
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-9982R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9982R-A750
Lokale Artikelnummer::
BOSSBS-9982R-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 C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.
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
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
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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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