Suche >
N\\\'-[1-Cyclopropylaminopropylidene]hydrazinecarboxylic+acid-ter
Drucken
Sie suchten nach:
23 835 results were found
N\\\'-[1-Cyclopropylaminopropylidene]hydrazinecarboxylic+acid-ter
Artikel-Nr:
(BOSSBS-12321R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12321R-CY7
Lokale Artikelnummer::
BOSSBS-12321R-CY7
Beschreibung:
Tect3 is a 607 amino acid single-pass type I membrane protein that belongs to the tectonic family and exists as four alternatively spliced isoforms. Tect3 interacts with MKS1 and may be involved in apoptosis regulation. The gene that encodes Tect3 contains approximately 31,560 bases and maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs and encoding nearly 1,200 genes, chromosome 10 makes up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, Cockayne syndrome, multiple endocrine neoplasia type 2 and porphyria. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12321R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12321R-A680
Lokale Artikelnummer::
BOSSBS-12321R-A680
Beschreibung:
Tect3 is a 607 amino acid single-pass type I membrane protein that belongs to the tectonic family and exists as four alternatively spliced isoforms. Tect3 interacts with MKS1 and may be involved in apoptosis regulation. The gene that encodes Tect3 contains approximately 31560 bases and maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs and encoding nearly 1200 genes, chromosome 10 makes up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, Cockayne syndrome, multiple endocrine neoplasia type 2 and porphyria. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
Recognizes a protein of ~55 kDa, identified as SOX10. This MAb is highly specific and does not cross-react with other members of the SOX-family. SOX genes comprise a family of genes that are related to the mammalian sex-determining gene SRY. These genes similarly contain sequences that encode for the HMG-box domain, which is responsible for the sequence-specific DNA-binding activity. SOX-10 is a sensitive marker of melanoma, including conventional, spindled, and desmoplastic subtypes. It is expressed by metastatic melanomas and nodal capsular nevus in sentinel lymph nodes, but not by other lymph node components such as dendritic cells, which usually express S100 protein. Commonly used melanoma markers, such as anti-HMB-45 and anti-Melan-A, are poorly expressed in desmoplastic melanomas while SOX-10 is moderately to strongly expressed in desmoplastic melanomas. SOX-10 is considered as a very reliable marker for recognizing residual desmoplastic melanomas. In normal tissues, it is expressed in Schwann cells, melanocytes, and myoepithelial cells of salivary, bronchial and mammary glands. SOX-10 expression is also observed in mast cells.
Artikel-Nr:
(BOSSBS-12321R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12321R-CY5
Lokale Artikelnummer::
BOSSBS-12321R-CY5
Beschreibung:
Tect3 is a 607 amino acid single-pass type I membrane protein that belongs to the tectonic family and exists as four alternatively spliced isoforms. Tect3 interacts with MKS1 and may be involved in apoptosis regulation. The gene that encodes Tect3 contains approximately 31,560 bases and maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs and encoding nearly 1,200 genes, chromosome 10 makes up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, Cockayne syndrome, multiple endocrine neoplasia type 2 and porphyria. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8594R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-A350
Lokale Artikelnummer::
BOSSBS-8594R-A350
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Lieferant:
G-Biosciences
Beschreibung:
G-Biosciences' Destain I contains approximately 45% methanol and 9% glacial acetic acid. G-Biosciences' Destain II contains approximately 5% methanol and 7% acetic acid.
Artikel-Nr:
(E406-5ML)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRCE406-5ML
Beschreibung:
Ethidiumbromid in 0,625 mg/ml Tropfflasche. Ein Tropfen in 50 ml flüssiger Agarose oder Puffer verdünnt ergibt eine Endkonzentration von 0,5 μg/ml. In einer Konzentration von 0,5 μg/ml ist Ethidiumbromid zweckmäßig in Agarose- oder Acrylamidgelen für die Bandenfeststellung. Es ermöglicht die Detektion von Nukleinsäure in Mengen von lediglich 10 ng. In höheren Konzentrationen (0,5 - 1,0 μg/ml) kann es bei der Aufreinigung von DNA in einem Caesiumchlorid-Gradienten verwendet werden.
VE:
1 * 5 mL
Lieferant:
PanReac AppliChem
Beschreibung:
HEPES (2-[4-(2-Hydroxyethyl)-1-piperazinyl]ethansulfonsäure) ≥99,5% für die Molekularbiologie
Lieferant:
Corning
Beschreibung:
PET, clear.
Lieferant:
Alfa Aesar
Beschreibung:
Indium(III)acetylacetonat ≥98%
Lieferant:
BELLCO GLASS
Beschreibung:
Spinner Flask with caps (45 mm) for side arms, Kapazität: 3000 ml, Anzahl Seitenarme: 2, Ø×H: 165×280 mm
Lieferant:
MACHEREY-NAGEL
Beschreibung:
Septen, Silikon weiß/PTFE beige, Härte: 45° shore A, Stärke: 3,0 mm, Ø: 20 mm
Artikel-Nr:
(NICK625)
Lieferant:
NICKEL ELECTRO
Hersteller-Artikelnummer::
625
Lokale Artikelnummer::
NICK625
Beschreibung:
Dissecting trays made of aluminium.
VE:
1 * 1 ST
Artikel-Nr:
(AMARZ640830)
Lieferant:
AMARELL, ARNO
Hersteller-Artikelnummer::
Z640830
Lokale Artikelnummer::
AMARZ640830
Beschreibung:
Glasthermometer, Thermometer, fish shaped, +5...+45 °C, Länge: 155 mm, Füllung: Spirit (blue)
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
[1,1'-Bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride 98%
Artikel-Nr:
(BOSSBS-13140R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13140R
Lokale Artikelnummer::
BOSSBS-13140R
Beschreibung:
Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromsomal instability (1,2). The FA Group C complementation group gene encodes the protein FANCC, which is located in both cytoplasmic and nuclear compartments. FANCC is expressed in a cell cycle-dependent manner, with the lowest levels at the G1/S boundary and the highest levels in the M-phase. The FANCC protein interacts with other FA complementation group proteins as well as non-FA proteins (3). A human a spectrin II (designated aSpIIs) acts as a scaffold to enhance interactions between FANCC and FANCA to form a nuclear complex (4,5). Another binding partner of FANCC is the BTB/POZ domain containing protein FAZF, which is a transcriptional repressor (6). In hematopoietic cells expressing mutant FANCC, PKR is constitutively phosphorylated and has increased binding affinity for double-stranded RNA (7,8), which suggests that FANCC indirectly suppresses the activity of PKR. These cells are also apoptotic and are hypersensitive to IFNg and TNFa (8). In addition, FANCC protein is involved in the activation of STAT1 through receptors for at least three hematopoietic growth and survival factors (8).
VE:
1 * 100 µl
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
