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4,4-Dimethylcyclohexa-1,5-dienylboronsäure+Mononatriumsalz
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4,4-Dimethylcyclohexa-1,5-dienylboronsäure+Mononatriumsalz
Artikel-Nr:
(APOSOR471600-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR471600-100G
Lokale Artikelnummer::
APOSOR471600-100G
Beschreibung:
D-Valin-methylester-hydrochlorid 98%
VE:
1 * 100 g
Artikel-Nr:
(NALG322004-9050)
Lieferant:
Thermo Fisher Scientific
Hersteller-Artikelnummer::
322004-9050
Lokale Artikelnummer::
NALG322004-9050
Beschreibung:
Narrow mouth Boston round diagnostic bottle is made of opaque amber high-density polyethylene (HDPE) and comes with an opaque amber polypropylene closure.
VE:
1 * 1.500 ST
Artikel-Nr:
(ATLAESDTX350/44)
Lieferant:
ATLAS - the shoe company
Hersteller-Artikelnummer::
ESDTX350/44
Lokale Artikelnummer::
ATLAESDTX350/44
Beschreibung:
Leichter ESD-Sicherheitsschuh aus Sportline-Obermaterial (geöltes Nubukleder), atmungsaktivem Funktionsfutter und einer MPU® Light-Sohle (3,5 mm Profil, öl-, säure- und benzinbeständig, antistatisch).
VE:
1 * 1 PAAR
Artikel-Nr:
(BOSSBS-8237R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8237R-CY5
Lokale Artikelnummer::
BOSSBS-8237R-CY5
Beschreibung:
FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 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
Artikel-Nr:
(BOSSBS-8237R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8237R-A750
Lokale Artikelnummer::
BOSSBS-8237R-A750
Beschreibung:
FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 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-localised genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13222R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-HRP
Lokale Artikelnummer::
BOSSBS-13222R-HRP
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
Artikel-Nr:
(BOSSBS-13222R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-CY3
Lokale Artikelnummer::
BOSSBS-13222R-CY3
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
Artikel-Nr:
(BOSSBS-13222R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-A555
Lokale Artikelnummer::
BOSSBS-13222R-A555
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
Artikel-Nr:
(SCRR2.1311.01.44)
Lieferant:
SCHURR SCHUHVERTRIEB
Hersteller-Artikelnummer::
2.1311.01.44
Lokale Artikelnummer::
SCRR2.1311.01.44
Beschreibung:
Safety shoe made from smooth leather, padded collar and an anti-slip and anti-static 'A4' nitrile rubber sole; with adjustable heel strap.
VE:
1 * 1 PAAR
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4,6-Dichloro-2H-thiochromene-3-carbaldehyde
Artikel-Nr:
(APOSPC0295-50MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC0295-50MG
Lokale Artikelnummer::
APOSPC0295-50MG
Beschreibung:
2-Brom-4,5-bis(trifluormethyl)anilin
VE:
1 * 50 mg
Artikel-Nr:
(BOSSBS-11916R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11916R-CY3
Lokale Artikelnummer::
BOSSBS-11916R-CY3
Beschreibung:
Neugrin, also known as NGRN, mesenchymal stem cell protein DSC92, neurite outgrowth-associated protein or spinal cord-derived protein FI58G, is a 291 amino acid protein that plays a role in neuronal differentiation and belongs to the neugrin family. As both a secreted and nuclear protein, neugrin exists as two alternatively spliced isoforms and is highly expressed in skeletal muscle, brain and heart. Neugrin is upregulated in neuroblastostoma cells by retinoic acid treatment and is encoded by a gene that maps to human chromosome 15q26.1. Chromosome 15 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
Artikel-Nr:
(BOSSBS-11916R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11916R-CY5
Lokale Artikelnummer::
BOSSBS-11916R-CY5
Beschreibung:
Neugrin, also known as NGRN, mesenchymal stem cell protein DSC92, neurite outgrowth-associated protein or spinal cord-derived protein FI58G, is a 291 amino acid protein that plays a role in neuronal differentiation and belongs to the neugrin family. As both a secreted and nuclear protein, neugrin exists as two alternatively spliced isoforms and is highly expressed in skeletal muscle, brain and heart. Neugrin is upregulated in neuroblastostoma cells by retinoic acid treatment and is encoded by a gene that maps to human chromosome 15q26.1. Chromosome 15 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
Artikel-Nr:
(1006801.)
Lieferant:
USP
Hersteller-Artikelnummer::
1006801
Lokale Artikelnummer::
USPH1006801
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 3 ST
Artikel-Nr:
(BOSSBS-15422R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15422R-CY7
Lokale Artikelnummer::
BOSSBS-15422R-CY7
Beschreibung:
HCAP G is a subunit of the condensin complex, which is responsible for the condensation and stabilisation of chromosomes during mitosis and meiosis. Phosphorylation of the encoded protein activates the condensin complex. There are pseudogenes for this gene on chromosomes 8 and 15. Alternative splicing results in multiple transcript variants.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Empagliflozin 98%
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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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