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Artikel-Nr:
(USBI041830-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
041830-BIOTIN
Lokale Artikelnummer::
USBI041830-BIOTIN
Beschreibung:
Anti-SLC22A2 Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 µl
Lieferant:
Alfa Aesar
Beschreibung:
Tetrazoliumblauchlorid
Artikel-Nr:
(BOSSBS-12157R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12157R-A647
Lokale Artikelnummer::
BOSSBS-12157R-A647
Beschreibung:
The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a motif of eight cysteines. This gene product can exist either as a homodimer (PDGF-BB) or as a heterodimer with the platelet-derived growth factor alpha polypeptide (PDGF-AB), where the dimers are connected by disulfide bonds. Mutations in this gene are associated with meningioma. Reciprocal translocations between chromosomes 22 and 7, at sites where this gene and that for COL1A1 are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans resulting from unregulated expression of growth factor. Two alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12157R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12157R-A350
Lokale Artikelnummer::
BOSSBS-12157R-A350
Beschreibung:
The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a motif of eight cysteines. This gene product can exist either as a homodimer (PDGF-BB) or as a heterodimer with the platelet-derived growth factor alpha polypeptide (PDGF-AB), where the dimers are connected by disulfide bonds. Mutations in this gene are associated with meningioma. Reciprocal translocations between chromosomes 22 and 7, at sites where this gene and that for COL1A1 are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans resulting from unregulated expression of growth factor. Two alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9496R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9496R-A680
Lokale Artikelnummer::
BOSSBS-9496R-A680
Beschreibung:
C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukaemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12499R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12499R-HRP
Lokale Artikelnummer::
BOSSBS-12499R-HRP
Beschreibung:
The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-IV (apolipoprotein L-IV), also known as APOL4, is a 351 amino acid protein that exists as multiple alternatively spliced isoforms, one of which is secreted. Expressed in spleen, placenta, spinal cord, uterus, testis and trachea, apoL-IV is thought to play a role in lipid exchange and transport throughout the body and may be involved in reverse cholesterol transport, specifically from peripheral cells to the liver. Overexpression of apoL-IV is associated with schizophrenia, suggesting that apoL-IV may play a role in the pathogenesis of neural disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9656R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9656R-A350
Lokale Artikelnummer::
BOSSBS-9656R-A350
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9656R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9656R-A488
Lokale Artikelnummer::
BOSSBS-9656R-A488
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9497R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9497R-A555
Lokale Artikelnummer::
BOSSBS-9497R-A555
Beschreibung:
C9orf152 is a 239 amino acid protein encoded by a gene that maps to human chromosome 9q31.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9656R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9656R-A680
Lokale Artikelnummer::
BOSSBS-9656R-A680
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukaemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9494R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9494R-A647
Lokale Artikelnummer::
BOSSBS-9494R-A647
Beschreibung:
C9orf114 is a 376 amino acid protein encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(1175773.)
Lieferant:
USP
Hersteller-Artikelnummer::
1175773
Lokale Artikelnummer::
USPH1175773
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 200 mg
Artikel-Nr:
(ABNOPAB8379)
Lieferant:
Abnova
Hersteller-Artikelnummer::
PAB8379
Lokale Artikelnummer::
ABNOPAB8379
Beschreibung:
Sheep polyclonal antibody raised against Tacrolimus(22).
VE:
1 * 1 mg
Lieferant:
JULABO GmbH
Beschreibung:
Kalibrier-Thermostate sind für Anwendungen in Kalibrierlaboren, wie z. B. ISO, DKD, NAMAS, UKAS, und für Anforderungen gemäß DIN EN ISO 9001:2000 vorgesehen. Die Einheiten verfügen über eine Kammer mit konstanter Temperatur und eignen sich zur präzisen Kalibrierung von Temperatursensoren, Messgeräten und Thermometern gemäß nationaler und internationaler Standards. Die Modelle mit Kältemaschine eignen sich für alle Temperaturen von –30 bis +200 °C sowie als Kalibrier-Thermostate für Temperaturen von 50 bis 300 °C. Der optionale Präzisions-Referenzsensor ermöglicht das Messen von Referenztemperaturen. Die Bäder sind mit einer PID-Kaskaden-Temperaturregelung für höchste interne und externe Temperaturkonstanz und einem integrierten Programmgeber für 10 Programmschritte ausgestattet.
Lieferant:
MOTIC
Beschreibung:
Accessory for microscopes, Motic Deckgläser 22×22 mm (100 Einheiten)
Artikel-Nr:
(PRSI2497P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
2497P
Lokale Artikelnummer::
PRSI2497P
Beschreibung:
IL-22 receptor peptide is used for blocking the activity of IL-22 receptor antibody.
VE:
1 * 50 µG
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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