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1,1-Diphenylhydrazin+Hydrochlorid
Artikel-Nr:
(NABELM095K1ANLGZ)
Lieferant:
NABERTHERM
Hersteller-Artikelnummer::
LM095K1ANLGZ
Lokale Artikelnummer::
NABELM095K1ANLGZ
Beschreibung:
Muffelofen L9/11/SKM/B510 TMX1100 Klapptr 1 * 1 ST
VE:
1 * 1 ST
Artikel-Nr:
(NABELM095K1ANLTZ1)
Lieferant:
NABERTHERM
Hersteller-Artikelnummer::
LM095K1ANLTZ1
Lokale Artikelnummer::
NABELM095K1ANLTZ1
Beschreibung:
Muffelofen L9/11/SKM/B510 TMX1100 Klapptr 1 * 1 ST
VE:
1 * 1 ST
Artikel-Nr:
(NABELM095H1ANOGTZ1)
Lieferant:
NABERTHERM
Hersteller-Artikelnummer::
LM095H1ANOGTZ1
Lokale Artikelnummer::
NABELM095H1ANOGTZ1
Beschreibung:
Muffelofen LT9/11/SKM/C550 TMX1100 Hubtr 1 * 1 ST
VE:
1 * 1 ST
Artikel-Nr:
(ANSER065110)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
R065110
Lokale Artikelnummer::
ANSER065110
Beschreibung:
HANDSCHUH R-FLEX RINGERS R065 GR.11 1 * 12 PAAR
VE:
1 * 12 PAAR
Artikel-Nr:
(APOSOR1011388-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1011388-25G
Lokale Artikelnummer::
APOSOR1011388-25G
Beschreibung:
4’,4’’’,4’’’’’-Nitrilotris(([1,1’-Biphenyl]-4-Carboxylic Acid)) 25g pack 1 * 25 g
VE:
1 * 25 g
New Product
Artikel-Nr:
(APOSOR1014899-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1014899-1G
Lokale Artikelnummer::
APOSOR1014899-1G
Beschreibung:
S-3,3’-Bis(Phenyl)-1,1’-Bi-2-Naphthol 1g pack 1 * 1 g
VE:
1 * 1 g
New Product
Artikel-Nr:
(APOSOR1015251-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1015251-100G
Lokale Artikelnummer::
APOSOR1015251-100G
Beschreibung:
Trans-[4’-Butyl-1,1’-Bicyclohexyl]-4-One 100g pack 1 * 100 g
VE:
1 * 100 g
New Product
Artikel-Nr:
(ANSERIG0011BUL110)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
RIG0011BUL110
Lokale Artikelnummer::
ANSERIG0011BUL110
Beschreibung:
HANDSCHUH ACTIVARMR INSULATING CL.00 11 1 * 10 PAAR
VE:
1 * 10 PAAR
Artikel-Nr:
(BOSSBS-12068R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A350
Lokale Artikelnummer::
BOSSBS-12068R-A350
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9935R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9935R-A750
Lokale Artikelnummer::
BOSSBS-9935R-A750
Beschreibung:
C11orf16 is a 404 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12479R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12479R-HRP
Lokale Artikelnummer::
BOSSBS-12479R-HRP
Beschreibung:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A647
Lokale Artikelnummer::
BOSSBS-12068R-A647
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9932R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9932R-A680
Lokale Artikelnummer::
BOSSBS-9932R-A680
Beschreibung:
C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A555
Lokale Artikelnummer::
BOSSBS-12068R-A555
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-CY3
Lokale Artikelnummer::
BOSSBS-12068R-CY3
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12479R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12479R-A488
Lokale Artikelnummer::
BOSSBS-12479R-A488
Beschreibung:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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.
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