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3,3\'-Iminobis(propylamin)
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3,3\'-Iminobis(propylamin)
Artikel-Nr:
(BOSSBS-4222R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4222R
Lokale Artikelnummer::
BOSSBS-4222R
Beschreibung:
Subunit of the 11S REG-gamma (also called PA28-gamma) proteasome regulator, a donut-shaped homoheptamer which associates with the proteasome. 11S REG-gamma activates the trypsin-like catalytic subunit of the proteasome but inhibits the chymotrypsin-like and postglutamyl-preferring (PGPH) subunits. Facilitates the MDM2-TP53/p53 interaction which promotes ubiquitination- and MDM2-dependent proteasomal degradation of TP53/p53, limiting its accumulation and resulting in inhibited apoptosis after DNA damage. May also be involved in cell cycle regulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8199R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-A647
Lokale Artikelnummer::
BOSSBS-8199R-A647
Beschreibung:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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
Lieferant:
Alfa Aesar
Beschreibung:
Rubidiumchlorid ≥99% (Metall-Basis)
Artikel-Nr:
(BLDPBD208184-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD208184-1G
Lokale Artikelnummer::
BLDPBD208184-1G
Beschreibung:
Dimethyl(N,N,N',N'-tetramethylethylenediamine)palladium(II) 98%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Bromo-5-(trifluoromethyl)pyrazole
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Trifluoromethylthio)phenacyl bromide
Artikel-Nr:
(44917.KG)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
44917.KG
Lokale Artikelnummer::
ALFA44917.KG
Beschreibung:
Bornitrid ≥99,5% (Metall-Basis)
VE:
1 * 1 ST
Lieferant:
Alfa Aesar
Beschreibung:
Kaliumiodid ≥99%
Artikel-Nr:
(44838.KG)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
44838.KG
Lokale Artikelnummer::
ALFA44838.KG
Beschreibung:
Bornitrid ≥99,5% (Metall-Basis)
VE:
1 * 1 ST
Lieferant:
Alfa Aesar
Beschreibung:
2,3,4-Trimethoxybenzoesäure ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Fluor-3-nitroanilin
Artikel-Nr:
(BOSSBS-13190R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13190R-CY7
Lokale Artikelnummer::
BOSSBS-13190R-CY7
Beschreibung:
Fas ligand associated factor 1; Fas ligand-associated factor 1; FBP 11; FBP11; FLAF 1; FLAF1; FNBP 3; Formin binding protein 11; Formin binding protein 3; Formin-binding protein 11; Formin-binding protein 3; HIP-10; HIP10; Huntingtin interacting protein A; Huntingtin interacting protein HYPA; Huntingtin yeast partner A; Huntingtin-interacting protein 10; Huntingtin-interacting protein A; HYPA; NY REN 6; NY REN 6 antigen; PR40A_HUMAN; Pre mRNA processing factor 40 homolog A; Pre-mRNA-processing factor 40 homolog A; PRP40 pre mRNA processing factor 40 homolog A (S cerevisiae); PRP40 pre mRNA processing factor 40 homolog A (yeast); PRP40 pre mRNA processing factor 40 homolog A; PRPF 40A; PRPF40A; Renal carcinoma antigen NY-REN-6.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13190R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13190R-A488
Lokale Artikelnummer::
BOSSBS-13190R-A488
Beschreibung:
Fas ligand associated factor 1; Fas ligand-associated factor 1; FBP 11; FBP11; FLAF 1; FLAF1; FNBP 3; Formin binding protein 11; Formin binding protein 3; Formin-binding protein 11; Formin-binding protein 3; HIP-10; HIP10; Huntingtin interacting protein A; Huntingtin interacting protein HYPA; Huntingtin yeast partner A; Huntingtin-interacting protein 10; Huntingtin-interacting protein A; HYPA; NY REN 6; NY REN 6 antigen; PR40A_HUMAN; Pre mRNA processing factor 40 homolog A; Pre-mRNA-processing factor 40 homolog A; PRP40 pre mRNA processing factor 40 homolog A (S cerevisiae); PRP40 pre mRNA processing factor 40 homolog A (yeast); PRP40 pre mRNA processing factor 40 homolog A; PRPF 40A; PRPF40A; Renal carcinoma antigen NY-REN-6.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9659R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-FITC
Lokale Artikelnummer::
BOSSBS-9659R-FITC
Beschreibung:
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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9659R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A488
Lokale Artikelnummer::
BOSSBS-9659R-A488
Beschreibung:
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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9659R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A680
Lokale Artikelnummer::
BOSSBS-9659R-A680
Beschreibung:
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' 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterisation.
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.
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