BEL-ART
Artikel-Nr:
(BOSSBS-12217R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12217R-A350
Lokale Artikelnummer::
BOSSBS-12217R-A350
Beschreibung:
Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Krüppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. As a member of the krueppel C2H2-type zinc-finger protein family, ZNF263 (Zinc finger protein 263), also known as FPM315 or ZKSCAN12 (Zinc finger protein with KRAB and SCAN domains 12), is a 683 amino acid nuclear protein that contains nine C2H2-type zinc fingers, one KRAB domain and one SCAN box domain. ZNF263 acts as a transcriptional repressor in the nucleus and is expressed in various tissues including heart, brain, placenta, lung, liver, skeletal muscle, kidney, pancreas, spleen, thymus, prostate, testis, ovary, small intestine, colon and leukocyte.
VE:
1 * 100 µl
Artikel-Nr:
(720-1867)
Lieferant:
Simport Scientific
Hersteller-Artikelnummer::
M965-40
Lokale Artikelnummer::
SIMPM965-40
Beschreibung:
Der CytoSep™ MEGA Trichter bietet eine einfache, effiziente und kostengünstige Möglichkeit zur Herstellung von hochwertigen Dünnschicht-Objektträgerpräparaten. Edelstahlklemmen sind nicht länger erforderlich, wodurch der Arbeitsablauf im Labor verbessert wird. Er eignet sich für die bequeme Vorbereitung von größeren Probenvolumen. Dieser größere Trichter ist schnell und einfach zu entfernen. Der große rechteckige Aufbringbereich für Zellen von 22×14,75 mm (325 mm²) ermöglicht ein 12-mal größeres Probenvolumen (6 ml) im Vergleich zum einfachen CytoSep™ Zytologie-Trichter. Mit ihm lassen sich im Vergleich zu anderen Dünnschichtmethoden kostengünstigere Dünnschicht-Präparate herstellen. Strategisch platzierte Leitbleche verhindern die Zellablagerung, so dass eine gleichmäßige Zellverteilung erreicht wird und damit hochwertige Objektträgerpräparate erstellt werden. CytoSep™ MEGA Zytologie-Trichter mit Deckel minimieren den Kontakt der Benutzer mit Pathogenen und verringern die Gefahr einer Kreuzkontamination der Proben. Zur Vorbereitung von lufttrockenen und fixierten Präparaten.
VE:
1 * 480 ST
Lieferant:
HAMMACHER KARL
Beschreibung:
Double ended, broad spoon spatulas made of WIRONIT steel (stainless steel 18/12 with 18% chrome and 10 to 12% nickel).
Artikel-Nr:
(472060050.)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
472060050
Lokale Artikelnummer::
ACRO472060050
Beschreibung:
Olsalazine Sodium 98%
VE:
1 * 5 g
New Product
Artikel-Nr:
(BINH1000145)
Lieferant:
Binhold, Paul Lehrmittel
Hersteller-Artikelnummer::
1000145
Lokale Artikelnummer::
BINH1000145
Beschreibung:
This spinal replica consists of the 12 thoracic vertebrae with intervertebral discs, thoracic nerves and spinal cord.
VE:
1 * 1 ST
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Artikel-Nr:
(MOLE64133332-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
64133332-100G
Lokale Artikelnummer::
MOLE64133332-100G
Beschreibung:
3-Nitrophthalsäure
VE:
1 * 100 g
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Lieferant:
Biotium
Beschreibung:
Recognizes the L1 or Calprotectin molecule, an intra-cytoplasmic antigen comprising of a 12 kDa alpha chain and a 14 kDa beta chain. Calprotectin comprises 60% of the cytoplasmic protein fraction of circulating polymorphonuclear granulocytes and is also found in monocytes, macrophages and ileal tissue eosinophils. Peripheral blood monocytes carry the antigen extra- and intracellularly, neutrophils only intracellularly. Calprotectin has antibacterial, antifungal, immunomodulating and antiproliferative effects. Besides this it is a potent chemotactic factor for neutrophils. Plasma concentrations are elevated in diseases associated with increased neutrophil activity, like inflammatory bowel disease. Granulocytes terminate their existence after transmigration through the intestinal wall. Therefore calprotectin is also detectable in feces. Elevated levels of calprotectin have been observed in body fluids such as plasma, saliva, gingival crevicular fluid, stools, and synovial fluid during infection and inflammatory conditions.This MAb reacts with neutrophils, monocytes, macrophages, and squamous mucosal epithelia and is important for identifying macrophages in tissue sections.
Artikel-Nr:
(BOSSBS-15154R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15154R-A750
Lokale Artikelnummer::
BOSSBS-15154R-A750
Beschreibung:
C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15154R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15154R-A555
Lokale Artikelnummer::
BOSSBS-15154R-A555
Beschreibung:
C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:
1 * 100 µl
Lieferant:
Bel-Art Products, a Part of SP
Beschreibung:
Polyoxymethylen, farbig
Artikel-Nr:
(SOEH1009152)
Lieferant:
SOEHNGEN
Hersteller-Artikelnummer::
1009152
Lokale Artikelnummer::
SOEH1009152
Beschreibung:
Verschiedene Fingerverbände für kleine Wunden. Ideal für die Verwendung unterwegs.
VE:
1 * 1 ST
Artikel-Nr:
(WITG4.940.002)
Lieferant:
WITEG LABORTECHNIK
Hersteller-Artikelnummer::
4.940.002
Lokale Artikelnummer::
WITG4.940.002
Beschreibung:
DURAN®, borosilicate glass.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11604R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-HRP
Lokale Artikelnummer::
BOSSBS-11604R-HRP
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5827R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5827R-A555
Lokale Artikelnummer::
BOSSBS-5827R-A555
Beschreibung:
PCDHGB5 is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11604R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-A350
Lokale Artikelnummer::
BOSSBS-11604R-A350
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Lieferant:
Serva
Beschreibung:
Phenolrot
Preis auf Anfrage
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