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Tris(4-bromophenyl)amine
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Tris(4-bromophenyl)amine
Artikel-Nr:
(238-1101)
Lieferant:
WIHA WERKZEUGE WILLI HAHN
Hersteller-Artikelnummer::
02292
Lokale Artikelnummer::
WIHA02292
Beschreibung:
These matt chrome-plated keys have a hexagonal ball end.
VE:
1 * 1 SET
Lieferant:
WIHA WERKZEUGE WILLI HAHN
Beschreibung:
High quality chrome-vanadium-molybdenum steel blade. Ideal for fine and delicate fastening tasks for electronics, precision mechanics, model-making and hobby activities.
Artikel-Nr:
(USBIR1424-95C-10)
Lieferant:
US Biological
Hersteller-Artikelnummer::
R1424-95C-10
Lokale Artikelnummer::
USBIR1424-95C-10
Beschreibung:
Anti-Relaxin 1 Mouse Monoclonal Antibody [clone: willi: ]
VE:
1 * 10 µG
Artikel-Nr:
(S7521-10EA)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
S7521-10EA
Lokale Artikelnummer::
SUPLS7521-10EA
Beschreibung:
Made of nylon.
VE:
1 * 10 ST
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
Plugs, Bohrung Ø: 4,0 mm, Hahn: 18,8 NS, Für: Hähne, gerade Bohrung, Ersatz-Hahnküken, PTFE
Artikel-Nr:
(612-7206)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI612-7206
Beschreibung:
VWR®, Spare stopcock for burettes 612-6694, 612-6695 and 612-6696
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-13326R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-CY3
Lokale Artikelnummer::
BOSSBS-13326R-CY3
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-13326R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-A350
Lokale Artikelnummer::
BOSSBS-13326R-A350
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-8654R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R-FITC
Lokale Artikelnummer::
BOSSBS-8654R-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 FAM81A gene product has been provisionally designated FAM81A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9625R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9625R-A680
Lokale Artikelnummer::
BOSSBS-9625R-A680
Beschreibung:
This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9625R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9625R-A750
Lokale Artikelnummer::
BOSSBS-9625R-A750
Beschreibung:
This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8578R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-HRP
Lokale Artikelnummer::
BOSSBS-8578R-HRP
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-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-CY5.5
Lokale Artikelnummer::
BOSSBS-8578R-CY5.5
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-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A647
Lokale Artikelnummer::
BOSSBS-8578R-A647
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-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
Artikel-Nr:
(BOSSBS-13222R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13222R-A647
Lokale Artikelnummer::
BOSSBS-13222R-A647
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
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.
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