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1,8-Dihydroxynaphthalin
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1,8-Dihydroxynaphthalin
Lieferant:
Cayman Chemical
Beschreibung:
CCVJ is a fluorescent molecular rotor characterised by low background fluorescence, low fluorescence anisotropy, and good water solubility. Fluorescent molecular rotors are molecules whose fluorescence is inversely proportional to its intramolecular rotation.
Artikel-Nr:
(KRAF10065.7021)
Lieferant:
Bernd Kraft
Hersteller-Artikelnummer::
10065.7021
Lokale Artikelnummer::
KRAF10065.7021
Beschreibung:
Schwefelsäure 0.9 mol/l (1.8 N) in wässriger Lösung
VE:
1 * 19 L
Artikel-Nr:
(BOSSBS-10037R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10037R-A750
Lokale Artikelnummer::
BOSSBS-10037R-A750
Beschreibung:
This gene encodes a subunit of the transcription factor complex nuclear factor-kappa-B (NFkB). The NFkB complex is expressed in numerous cell types and functions as a central activator of genes involved in inflammation and immune function. The protein encoded by this gene can function as both a transcriptional activator or repressor depending on its dimerization partner. The p100 full-length protein is co-translationally processed into a p52 active form. Chromosomal rearrangements and translocations of this locus have been observed in B cell lymphomas, some of which may result in the formation of fusion proteins. There is a pseudogene for this gene on chromosome 18. Alternative splicing results in multiple transcript variants.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8098R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8098R-A680
Lokale Artikelnummer::
BOSSBS-8098R-A680
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC34 (coiled-coil domain containing 34), also known as Renal carcinoma antigen NY-REN-41, is a 373 amino acid protein that is expressed in testis, breast, lung, placenta, liver and small intestine. A translocation between the short arms of chromosomes 11 and 18 affecting the CCDC34 gene has been identified in a patient with hamartoma of the retinal pigment epithelium. There are two isoforms of CCDC34 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8098R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8098R-A647
Lokale Artikelnummer::
BOSSBS-8098R-A647
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC34 (coiled-coil domain containing 34), also known as Renal carcinoma antigen NY-REN-41, is a 373 amino acid protein that is expressed in testis, breast, lung, placenta, liver and small intestine. A translocation between the short arms of chromosomes 11 and 18 affecting the CCDC34 gene has been identified in a patient with hamartoma of the retinal pigment epithelium. There are two isoforms of CCDC34 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12937R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12937R-A350
Lokale Artikelnummer::
BOSSBS-12937R-A350
Beschreibung:
CTBS is an evolutionarily conserved member of the glycosyl hydrolase 18 family of proteins. Localizing to the lysosome, CTBS plays a role in the degradation of asparagine-linked (Asn-linked) glycoproteins. Glycoproteins are translocated to lysosomes via endocytosis or autophagy where they are broken down by proteases and glycosidases. The catabolism of glycoproteins is an important step in the regular turnover of cellular contents and in maintaining the homeostasis of glycosylation. CTBS functions as a glycosidase that cleaves the reducing end GlcNAc from the core chitobiase unit of oligosaccharides. Before this reaction can occur, AGA (the lysosomal glycosylasparaginase) must first remove the Asn from the Asn-linked glycoprotein to expose the reducing end GlcNAc, thereby allowing CTBS to access the exposed moiety.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12937R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12937R-CY7
Lokale Artikelnummer::
BOSSBS-12937R-CY7
Beschreibung:
CTBS is an evolutionarily conserved member of the glycosyl hydrolase 18 family of proteins. Localizing to the lysosome, CTBS plays a role in the degradation of asparagine-linked (Asn-linked) glycoproteins. Glycoproteins are translocated to lysosomes via endocytosis or autophagy where they are broken down by proteases and glycosidases. The catabolism of glycoproteins is an important step in the regular turnover of cellular contents and in maintaining the homeostasis of glycosylation. CTBS functions as a glycosidase that cleaves the reducing end GlcNAc from the core chitobiase unit of oligosaccharides. Before this reaction can occur, AGA (the lysosomal glycosylasparaginase) must first remove the Asn from the Asn-linked glycoprotein to expose the reducing end GlcNAc, thereby allowing CTBS to access the exposed moiety.
VE:
1 * 100 µl
Artikel-Nr:
(444-0695)
Lieferant:
GRANT INSTRUMENTS
Hersteller-Artikelnummer::
PTR-35
Lokale Artikelnummer::
GRANPTR-35
Beschreibung:
Die Multifunktionsrotatoren PTR-35 und PTR-60 mit variabler Geschwindigkeit, variablem Winkel und 360° bieten flexible Mischoptionen in einer kompakten Einheit. Zu den Anwendungen gehören das Mischen von Mikroröhrchen, Immunpräzipitation und andere Affinitätsmatrixanwendungen, die Verhinderung von Blutgerinnung und Latexdiagnostik. Der Schrittmotor erzeugt eine geregelte und reproduzierbare Rotation über den gesamten Geschwindigkeitsbereich. Die Rotatoren bieten alles, was zum Mischen unterschiedlich großer Partikel erforderlich ist.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-8098R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8098R-A555
Lokale Artikelnummer::
BOSSBS-8098R-A555
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC34 (coiled-coil domain containing 34), also known as Renal carcinoma antigen NY-REN-41, is a 373 amino acid protein that is expressed in testis, breast, lung, placenta, liver and small intestine. A translocation between the short arms of chromosomes 11 and 18 affecting the CCDC34 gene has been identified in a patient with hamartoma of the retinal pigment epithelium. There are two isoforms of CCDC34 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11190R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11190R-CY5
Lokale Artikelnummer::
BOSSBS-11190R-CY5
Beschreibung:
C9 is a plasma protein synthesized in the liver and monocytes consisting of a single polypeptide chain. C9 is a part of the membrane attack complex (MAC), an important component of the immune system. The MAC forms upon complement system activation by invading pathogenic bacteria and consists of the four major complement proteins: C5b, C6, C7 and C8. These complement proteins bind to the outer surface of the plasma membrane of the invading cell. C9 binds to the membrane associated C5b-8 protein, which leads to the circular polymerization of 12-18 C9 molecules. These polymerized C9 molecules form a ring structure in the membrane. Molecules can then diffuse freely through this transmembrane channel, causing cell lysis and destruction of the invading bacterial cell.
VE:
1 * 100 µl
Lieferant:
Agilent
Beschreibung:
18 ml vials
Artikel-Nr:
(BOSSBS-2984R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2984R-HRP
Lokale Artikelnummer::
BOSSBS-2984R-HRP
Beschreibung:
Defects in PLN are the cause of cardiomyopathy dilated type 1P (CMD1P) . Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.Defects in PLN are the cause of cardiomyopathy familial hypertrophic type 18 (CMH18) . CMH18 is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2984R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2984R-A555
Lokale Artikelnummer::
BOSSBS-2984R-A555
Beschreibung:
Defects in PLN are the cause of cardiomyopathy dilated type 1P (CMD1P) . Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.Defects in PLN are the cause of cardiomyopathy familial hypertrophic type 18 (CMH18) . CMH18 is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12937R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12937R
Lokale Artikelnummer::
BOSSBS-12937R
Beschreibung:
CTBS is an evolutionarily conserved member of the glycosyl hydrolase 18 family of proteins. Localizing to the lysosome, CTBS plays a role in the degradation of asparagine-linked (Asn-linked) glycoproteins. Glycoproteins are translocated to lysosomes via endocytosis or autophagy where they are broken down by proteases and glycosidases. The catabolism of glycoproteins is an important step in the regular turnover of cellular contents and in maintaining the homeostasis of glycosylation. CTBS functions as a glycosidase that cleaves the reducing end GlcNAc from the core chitobiase unit of oligosaccharides. Before this reaction can occur, AGA (the lysosomal glycosylasparaginase) must first remove the Asn from the Asn-linked glycoprotein to expose the reducing end GlcNAc, thereby allowing CTBS to access the exposed moiety.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12937R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12937R-CY3
Lokale Artikelnummer::
BOSSBS-12937R-CY3
Beschreibung:
CTBS is an evolutionarily conserved member of the glycosyl hydrolase 18 family of proteins. Localizing to the lysosome, CTBS plays a role in the degradation of asparagine-linked (Asn-linked) glycoproteins. Glycoproteins are translocated to lysosomes via endocytosis or autophagy where they are broken down by proteases and glycosidases. The catabolism of glycoproteins is an important step in the regular turnover of cellular contents and in maintaining the homeostasis of glycosylation. CTBS functions as a glycosidase that cleaves the reducing end GlcNAc from the core chitobiase unit of oligosaccharides. Before this reaction can occur, AGA (the lysosomal glycosylasparaginase) must first remove the Asn from the Asn-linked glycoprotein to expose the reducing end GlcNAc, thereby allowing CTBS to access the exposed moiety.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
Reacts with a protein of 57 kDa, identified as the L1 protein of human papilloma virus type 16 (HPV-16). It is the major capsid protein of HPV-16. Infection with specific types of HPV has been associated with an increased risk of developing cervical neoplasia. HPV types 6 and 11 have been associated with relatively benign diseases such as genital warts but types 16 and 18 are strongly associated with cervical, vaginal, and vulvar malignancies. The antibody reacts very strongly with formalin-fixed, paraffin-embedded tissues containing HPV-16 or -33; very weak reactions were occasionally observed with biopsy specimens or smears containing HPV-6 or HPV-11. It cross-reacts with HPV37.
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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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