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Amberlyst\\\\\\\\u00AE+15
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-(2-Fluorophenyl)-2-piperidone 95%
Artikel-Nr:
(479-0849)
Lieferant:
TENAK
Hersteller-Artikelnummer::
TE25208
Lokale Artikelnummer::
TENATE25208
Beschreibung:
Edelstahl, ausziehbarer Einschub.
VE:
1 * 1 ST
Lieferant:
DWK Life Sciences
Beschreibung:
Schraubverschluss aus strahlungsbeständigem Polypropylen.
Lieferant:
Thermo Scientific
Beschreibung:
(+)-cis-Diltiazem hydrochloride 98%
Artikel-Nr:
(BOSSBS-9626R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-FITC
Lokale Artikelnummer::
BOSSBS-9626R-FITC
Beschreibung:
RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9626R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-A647
Lokale Artikelnummer::
BOSSBS-9626R-A647
Beschreibung:
RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9626R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-HRP
Lokale Artikelnummer::
BOSSBS-9626R-HRP
Beschreibung:
RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Lieferant:
BIOMOL RESEARCH LABORATORIES
Beschreibung:
Hydroxyectoin
Artikel-Nr:
(442-4522)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI442-4522
Beschreibung:
<B>PTFE</B>-ummantelter, starker Alnico V-Magnetkern. Abgerundete, glatte Oberfläche.
VE:
1 * 10 ST
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
8-Nitroquinolin-3-amine 95%
Artikel-Nr:
(BOSSBS-8654R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R-A555
Lokale Artikelnummer::
BOSSBS-8654R-A555
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13326R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-FITC
Lokale Artikelnummer::
BOSSBS-13326R-FITC
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11012R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-A555
Lokale Artikelnummer::
BOSSBS-11012R-A555
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is 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. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
2-Nitrobenzamid ≥98%
Artikel-Nr:
(HECH40624010)
Lieferant:
GLASWARENFABRIK KARL HECHT
Hersteller-Artikelnummer::
40624010
Lokale Artikelnummer::
HECH40624010
Beschreibung:
Glass spot plates with 10 or 12 numbered cavities. For flocculation tests.
VE:
1 * 1 ST
Artikel-Nr:
(APOSOR51827-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR51827-1G
Lokale Artikelnummer::
APOSOR51827-1G
Beschreibung:
2,6-Dimethoxypyrazine
VE:
1 * 1 g
Preis auf Anfrage
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.
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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