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Benzoic+acid-acyl-\\u03B2-D-glucuronide
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Benzoic+acid-acyl-\\u03B2-D-glucuronide
Artikel-Nr:
(BOSSBS-8578R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-FITC
Lokale Artikelnummer::
BOSSBS-8578R-FITC
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. 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-8578R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-CY7
Lokale Artikelnummer::
BOSSBS-8578R-CY7
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. 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-8575R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-CY5
Lokale Artikelnummer::
BOSSBS-8575R-CY5
Beschreibung:
FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. 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:
Alfa Aesar
Beschreibung:
Formylglycin 98%
Artikel-Nr:
(BOSSBS-8578R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R
Lokale Artikelnummer::
BOSSBS-8578R
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. 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:
APOLLO SCIENTIFIC
Beschreibung:
Dimethallylamine 95%
Lieferant:
BELLINGHAM STANLEY
Beschreibung:
Handheld refractometers use high precision clear scale, and simple zero adjustment with lock.
Artikel-Nr:
(BOSSBS-9626R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R
Lokale Artikelnummer::
BOSSBS-9626R
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-CY3
Lokale Artikelnummer::
BOSSBS-9626R-CY3
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-8575R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-A488
Lokale Artikelnummer::
BOSSBS-8575R-A488
Beschreibung:
FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. 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:
(431-0205)
Lieferant:
KINEMATICA
Hersteller-Artikelnummer::
11030069
Lokale Artikelnummer::
KINE11030069
Beschreibung:
Dispergieraufsatz, PT-DA 20/2EC-E192, Für Gerät: PT 4000, Geschwindigkeit: 27 m/s, Stator/Rotor Ø: 15 / 20 mm, Volumen: 100 - 2500 ml
VE:
1 * 1 ST
Artikel-Nr:
(BLDPBD331216-5G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD331216-5G
Lokale Artikelnummer::
BLDPBD331216-5G
Beschreibung:
N-(4-Bromophenethyl)isobutyramide 97%
VE:
1 * 5 g
Artikel-Nr:
(211-7611)
Lieferant:
Bel-Art Products, a Part of SP
Hersteller-Artikelnummer::
F188380015
Lokale Artikelnummer::
BELAF188380015
Beschreibung:
These PP racks are available in different grid sizes that are with open sides which make them adaptable for use in a tray of crushed ice.
VE:
1 * 1 ST
Lieferant:
MIELE
Beschreibung:
Zubehör für Waschmaschinen für Glaswaren, DE-CS7-85 Gerätedeckel zur oberen Abdeckung der Maschine, B×T×H: 900×700×15 mm, Für: PG 8583 C
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Beschreibung:
Bietet eine Reihe von Selektivitäten mit unterschiedlichen Copolymerverhältnissen von PEG und Methylpolysiloxan. HI-PLUS, HI-PLUS 10, HI-PLUS 25, HI-PLUS 75, HI-PLUS 90.
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Beschreibung:
Bietet eine Reihe von Selektivitäten mit unterschiedlichen Copolymerverhältnissen von PEG und Methylpolysiloxan. HI-PLUS, HI-PLUS 10, HI-PLUS 25, HI-PLUS 75, HI-PLUS 90.
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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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