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Artikel-Nr:
(BOSSBS-9678R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9678R-A647
Lokale Artikelnummer::
BOSSBS-9678R-A647
Beschreibung:
C19orf21 is a 679 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9677R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9677R-A647
Lokale Artikelnummer::
BOSSBS-9677R-A647
Beschreibung:
C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9677R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9677R-CY3
Lokale Artikelnummer::
BOSSBS-9677R-CY3
Beschreibung:
C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9684R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9684R-CY7
Lokale Artikelnummer::
BOSSBS-9684R-CY7
Beschreibung:
C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9677R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9677R-FITC
Lokale Artikelnummer::
BOSSBS-9677R-FITC
Beschreibung:
C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9677R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9677R-A350
Lokale Artikelnummer::
BOSSBS-9677R-A350
Beschreibung:
C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Lieferant:
Agilent
Beschreibung:
Actuator limiter, 14-port, for LVO only
Lieferant:
SciLabware
Beschreibung:
Glass Stopper with 14/10 cone
Lieferant:
Thermo Scientific
Beschreibung:
Thermo Scientific Pierce BS3 (Sulfo-DSS) is bis(sulfosuccinimidyl)suberate, an amine-to-amine crosslinker that is homobifunctional, water-soluble, non-cleavable and membrane impermeable.
Lieferant:
Alfa Aesar
Beschreibung:
D(+)-Raffinose Pentahydrat ≥99%
Artikel-Nr:
(EHERC16173600)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C16173600
Lokale Artikelnummer::
EHERC16173600
Beschreibung:
Organic Standard, Phthalic acid, bis-isononyl ester
VE:
1 * 0,25 g
Artikel-Nr:
(ABCRAB123782.0001)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB123782.0001
Lokale Artikelnummer::
ABCRAB123782.0001
Beschreibung:
Metal Beta-diketonates, Metal TMHD, Volatile Precursors for CVD
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(ICNA0215202705)
Lieferant:
MP Biomedicals
Hersteller-Artikelnummer::
0215202705
Lokale Artikelnummer::
ICNA0215202705
Beschreibung:
Soluble in water (50 mg/mL - clear, faintly yellow solution).
VE:
1 * 5 mg
Lieferant:
Restek
Beschreibung:
Silylation derivatization reagent.
Artikel-Nr:
(256455-1)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
256455-1
Lokale Artikelnummer::
CALB256455-1
Beschreibung:
Desoxy-Big CHAP (N,N-Bis[3-(D-gluconamido)propyl]desoxycholamid), Calbiochem®
VE:
1 * 1 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Bortrifluorid-Methanol-Komplex 14% in Methanol, Sigma-Aldrich®
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.
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