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1,5-Diaminonaphthalin
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1,5-Diaminonaphthalin
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Beschreibung:
Allzwecksäule mit zusätzlicher Temperaturstabilität. Zur Analyse von Lösungsmittelverunreinigungen, PCBs, Kohlenwasserstoffen, ätherischen Ölen, halbflüchtigen Stoffen, Pestiziden, Phenolen usw.
Lieferant:
HIRSCHMANN
Beschreibung:
Einmalkapillaren für das Zentrifugieren von Blutproben.
Artikel-Nr:
(ENTEH60-50-0615)
Lieferant:
ENTEGRIS
Hersteller-Artikelnummer::
H60-50-0615
Lokale Artikelnummer::
ENTEH60-50-0615
Beschreibung:
Holds one mask or reticle.
VE:
1 * 25 ST
Artikel-Nr:
(BOSSBS-8578R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A555
Lokale Artikelnummer::
BOSSBS-8578R-A555
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-CY3
Lokale Artikelnummer::
BOSSBS-8575R-CY3
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:
(BOSSBS-8575R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-A750
Lokale Artikelnummer::
BOSSBS-8575R-A750
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:
(BOSSBS-8575R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R
Lokale Artikelnummer::
BOSSBS-8575R
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:
(BOSSBS-8578R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-CY3
Lokale Artikelnummer::
BOSSBS-8578R-CY3
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-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-CY5.5
Lokale Artikelnummer::
BOSSBS-8575R-CY5.5
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:
(BOSSBS-13560R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13560R-A680
Lokale Artikelnummer::
BOSSBS-13560R-A680
Beschreibung:
ZA20D3 is a zinc-finger protein located on chromosome 15. It is associated with PRK1.
VE:
1 * 100 µl
Artikel-Nr:
(99923.)
Lieferant:
Biotium
Hersteller-Artikelnummer::
99923
Lokale Artikelnummer::
BTIU99923
Beschreibung:
Firefly luciferase is widely used as a transcriptional reporter gene for research and drug screening. The Steady-Luc™ HTS kit can be used with luminescence plate readers without sample injection systems or for high-throughput screening.
VE:
1 * 15 mL
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,4-Di-O-acetyl-6-deoxy-L-glucal
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-Aminochinolin 98%
Artikel-Nr:
(APOSOR964112-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR964112-5G
Lokale Artikelnummer::
APOSOR964112-5G
Beschreibung:
6-Methoxy-1,2,3,4-tetrahydrochinolin 95%
VE:
1 * 5 g
Lieferant:
Avantor Fluid Handling
Beschreibung:
Geschmeidige Formulierung für Biegungen mit scharfem Radius.
Artikel-Nr:
(BOSSBS-13560R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13560R-A350
Lokale Artikelnummer::
BOSSBS-13560R-A350
Beschreibung:
ZA20D3 is a zinc-finger protein located on chromosome 15. It is associated with PRK1.
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.
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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