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3-(4-Hydroxyphenyl)benzonitril
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3-(4-Hydroxyphenyl)benzonitril
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Chlor-3,5-dinitro-α,α,α-trifluortoluol 99%
Artikel-Nr:
(BOSSBS-5218R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5218R-A555
Lokale Artikelnummer::
BOSSBS-5218R-A555
Beschreibung:
Acts as a negative regulator of entry into mitosis (G2 to M transition) by protecting the nucleus from cytoplasmically activated cyclin B1-complexed CDK1 before the onset of mitosis by mediating phosphorylation of CDK1 on 'Tyr-15'. Specifically phosphorylates and inactivates cyclin B1-complexed CDK1 reaching a maximum during G2 phase and a minimum as cells enter M phase. Phosphorylation of cyclin B1-CDK1 occurs exclusively on 'Tyr-15' and phosphorylation of monomeric CDK1 does not occur. Its activity increases during S and G2 phases and decreases at M phase when it is hyperphosphorylated. A correlated decrease in protein level occurs at M/G1 phase, probably due to its degradation.
VE:
1 * 100 µl
Artikel-Nr:
(22955.30)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
22955.30
Lokale Artikelnummer::
ALFA22955.30
Beschreibung:
Tungsten carbide cobalt ≥99% (Metall-Basis)
VE:
1 * 250 g
Artikel-Nr:
(CONTLWPN0020)
Lieferant:
CONTEC
Hersteller-Artikelnummer::
LWPN0020
Lokale Artikelnummer::
CONTLWPN0020
Beschreibung:
Ideal for wiping exterior surfaces of products and cleaning interior surfaces of process tools or other equipment. Made from 100% textured polyester no-run knit.
VE:
1 * 120 ST
Artikel-Nr:
(BOSSBS-8242R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-CY5.5
Lokale Artikelnummer::
BOSSBS-8242R-CY5.5
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8242R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-CY5
Lokale Artikelnummer::
BOSSBS-8242R-CY5
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD209395-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD209395-25G
Lokale Artikelnummer::
BLDPBD209395-25G
Beschreibung:
6-Chloro-5-fluoropyrimidin-4-amine 97%
VE:
1 * 25 g
Lieferant:
GREINER BIO ONE
Beschreibung:
In transparent PP or PS, with HDPE screw cap, sterile or non-sterile, round or conical bottom.
Artikel-Nr:
(BOSSBS-8242R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-A680
Lokale Artikelnummer::
BOSSBS-8242R-A680
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.
VE:
1 * 100 µl
Artikel-Nr:
(HONCR1846-100MG)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
R1846-100MG
Lokale Artikelnummer::
HONCR1846-100MG
Beschreibung:
Honeywell Fluka™ offers an expanding range of high quality inorganic certified reference materials and organic reference materials.
VE:
1 * 100 mg
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Aminoisonicotinsäure
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ph.Eur, Pyrogen free
Artikel-Nr:
(BOSSBS-13222R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-A680
Lokale Artikelnummer::
BOSSBS-13222R-A680
Beschreibung:
FSD2 is a 749 amino acid protein containing one B30.2/SPRY domain and two fibronectin type-III domains. The gene encoding FSD2 maps to human chromosome 15q25.2. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and consists of about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are also associated with chromosome 15.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,5-Dihydroxytoluol
Artikel-Nr:
(BOSSBS-9624R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9624R-CY5
Lokale Artikelnummer::
BOSSBS-9624R-CY5
Beschreibung:
Imp3, is a 184 amino acid protein that contains one S4 RNA-binding domain and is the mammalian homolog of the yeast Imp3 protein. Localized to the nucleus, Imp3 exists as a component of a heterotrimeric complex consisting of MPP10, Imp3 and Imp4 and, in this complex, plays a key role in early cleavage events during pre-18S ribosomal processing. The gene encoding Imp3 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
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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