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DIAGNOSTIC+SYSTEMS+DIASYS
Artikel-Nr:
(AVIVARP42946_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP42946_P050
Lokale Artikelnummer::
AVIVARP42946_P050
Beschreibung:
Anti-PEX2 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(AVIVARP65858_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP65858_P050
Lokale Artikelnummer::
AVIVARP65858_P050
Beschreibung:
Anti-BBS9 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(AVIVARP47633_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP47633_P050
Lokale Artikelnummer::
AVIVARP47633_P050
Beschreibung:
Anti-ZNF506 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(AVIVARP32336_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP32336_P050
Lokale Artikelnummer::
AVIVARP32336_P050
Beschreibung:
Anti-ISL1 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(AVIVARP65095_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP65095_P050
Lokale Artikelnummer::
AVIVARP65095_P050
Beschreibung:
Anti-PRICKLE2 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(AVIVARP58952_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP58952_P050
Lokale Artikelnummer::
AVIVARP58952_P050
Beschreibung:
Anti-SNX18 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(BOSSBS-12193R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12193R-A680
Lokale Artikelnummer::
BOSSBS-12193R-A680
Beschreibung:
Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly By similarity. Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promotes development of neural crest cells from neural tube progenitors. Restricts neural progenitor cells to the neural crest lineage while suppressing interneuron differentiation. Required for maintenance of pluripotent cells in the pre-implantation and peri-implantation stages of embryogenesis. Probable transcription factor involved in embryogenesis and somatogenesis. FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12193R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12193R-CY7
Lokale Artikelnummer::
BOSSBS-12193R-CY7
Beschreibung:
Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly By similarity. Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promotes development of neural crest cells from neural tube progenitors. Restricts neural progenitor cells to the neural crest lineage while suppressing interneuron differentiation. Required for maintenance of pluripotent cells in the pre-implantation and peri-implantation stages of embryogenesis. Probable transcription factor involved in embryogenesis and somatogenesis. FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13132R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-CY7
Lokale Artikelnummer::
BOSSBS-13132R-CY7
Beschreibung:
FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13132R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-CY5
Lokale Artikelnummer::
BOSSBS-13132R-CY5
Beschreibung:
FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
VE:
1 * 100 µl
Lieferant:
HemaCare
Beschreibung:
CD19<sup>+</sup> B cells are isolated from mononuclear cells by positive or negative selection using immunomagnetic cell separation procedures. Peripheral blood cells are collected from normal human volunteers by direct collection or by using the COBE® Spectra or Spectra Optia® Apheresis System where cell-rich leukapheresis product is extracted using continuous flow centrifugal technology directly into the collection bag.
Artikel-Nr:
(BOSSBS-1641R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1641R
Lokale Artikelnummer::
BOSSBS-1641R
Beschreibung:
The protein encoded by this gene has been termed a 'growth' or 'plasticity' protein because it is expressed at high levels in neuronal growth cones during development and axonal regeneration. This protein is considered a crucial component of an effective regenerative response in the nervous system. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10433R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10433R-CY3
Lokale Artikelnummer::
BOSSBS-10433R-CY3
Beschreibung:
Receptor for prostaglandin F2-alpha (PGF2-alpha). The activity of this receptor is mediated by G proteins which activate a phosphatidylinositol-calcium second messenger system. Initiates luteolysis in the corpus luteum (By similarity). Isoforms 2 to 7 do not bind PGF2-alpha but are proposed to modulate signaling by participating in variant receptor complexes; heterodimers between isoform 1 and isoform 5 are proposed to be a receptor for prostamides including the synthetic analog bimatoprost.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11204R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11204R
Lokale Artikelnummer::
BOSSBS-11204R
Beschreibung:
Transcription factor with important functions in the development of the eye, nose, central nervous system and pancreas. Required for the differentiation of pancreatic islet alpha cells (By similarity). Competes with PAX4 in binding to a common element in the glucagon, insulin and somatostatin promoters. Regulates specification of the ventral neuron subtypes by establishing the correct progenitor domains (By similarity). Isoform 5a appears to function as a molecular switch that specifies target genes.
VE:
1 * 100 µl
Artikel-Nr:
(AVIVARP63988_P050)
Lieferant:
Aviva Systems Biology
Hersteller-Artikelnummer::
ARP63988_P050
Lokale Artikelnummer::
AVIVARP63988_P050
Beschreibung:
Anti-DKFZp779C2259 Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Artikel-Nr:
(BOSSBS-11181R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11181R
Lokale Artikelnummer::
BOSSBS-11181R
Beschreibung:
This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. Mutations in this gene may be associated with autism and Asperger syndrome. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Oct 2009].
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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