4,4-Dimethylcyclohexa-1,5-dienylborons\u00E4ure+Mononatriumsalz
Artikel-Nr:
(BOSSBS-8578R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A350
Lokale Artikelnummer::
BOSSBS-8578R-A350
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-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A488
Lokale Artikelnummer::
BOSSBS-8578R-A488
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-8654R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R
Lokale Artikelnummer::
BOSSBS-8654R
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
Lieferant:
TENAK
Beschreibung:
Edelstahl.
Lieferant:
AESCULAP AG
Beschreibung:
Bone curette, type Simon (Fig. 00), with 4,4 mm end, Aesculap®
Lieferant:
Alfa Aesar
Beschreibung:
N-Methyl-4-nitroanilin ≥97%
Artikel-Nr:
(PRTWFW10BKR44)
Lieferant:
Portwest Clothing
Hersteller-Artikelnummer::
FW10BKR44
Lokale Artikelnummer::
PRTWFW10BKR44
Beschreibung:
Komfortabler, robuster und antistatischer Halbstiefel aus Büffelspaltleder mit einer öl- und hitzebeständigen (200 °C) Zweidichten-PU/PU-Laufsohle.
VE:
1 * 1 PAAR
Lieferant:
JULABO GmbH
Beschreibung:
Metal tubing is integrated insulated and flexible with connectors and fittings. This flexible metal tubing can be bolted together with the circulator and the external system, provides anti-slipping. Triple insulated tubing is used for wide temperature ranges.
Lieferant:
Ludwig Schneider GmbH & CO. KG
Beschreibung:
Rote oder blaue Füllung Beschichtung: PTFE / FEP, transparent
Lieferant:
Alfa Aesar
Beschreibung:
3-Fluoro-2-methylpyridine 98%
Lieferant:
COMBI-BLOCKS
Beschreibung:
Methylthiazol-5-carboxylat
Lieferant:
WTW
Beschreibung:
These special pH electrodes extend the range of the IDS series for enhanced applications in Life Sciences and related applications.
Artikel-Nr:
(PRTWFW02BLU44)
Lieferant:
Portwest Clothing
Hersteller-Artikelnummer::
FW02BLU44
Lokale Artikelnummer::
PRTWFW02BLU44
Beschreibung:
Low cut, S1P, hiker-style safety shoes, anti-static, with perforated cow suede leather upper plus a dual-density, oil resistant PU/PU outer sole.
VE:
1 * 1 PAAR
Artikel-Nr:
(BOSSBS-8575R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8575R-HRP
Lokale Artikelnummer::
BOSSBS-8575R-HRP
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:
COMBI-BLOCKS
Beschreibung:
(±)-1-Boc-3-hydroxypyrrolidin
Lieferant:
BIONET RESEARCH
Beschreibung:
4-Brom-2-methyl-6-nitroanilin
Preis auf Anfrage
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