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ELBE WERKSTATTEN
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2H-Perfluoro-5,8,11,14,17-pentamethyl-3,6,9,12,15,18-hexaoxahenicosane 95%
Artikel-Nr:
(BOSSBS-11505R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11505R-A647
Lokale Artikelnummer::
BOSSBS-11505R-A647
Beschreibung:
The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11505R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11505R-A488
Lokale Artikelnummer::
BOSSBS-11505R-A488
Beschreibung:
The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6318R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6318R-A350
Lokale Artikelnummer::
BOSSBS-6318R-A350
Beschreibung:
Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6318R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6318R-HRP
Lokale Artikelnummer::
BOSSBS-6318R-HRP
Beschreibung:
Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12311R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12311R-CY3
Lokale Artikelnummer::
BOSSBS-12311R-CY3
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. The primary function of these motifs is to provide a versatile structural framework to mediate the formation of protein-protein interactions. LRRs are present in a variety of proteins with diverse structure and function, including innate immunity and nervous system development. Several human diseases are associated with mutations in genes encoding LRR-containing proteins. LRRC23 (leucine-rich repeat-containing protein 23), also known as leucine-rich protein B7, is a 343 amino acid protein that contains eight LRR (leucine-rich) repeasts and one LRRCT domain. LRRC23 exists as two alternatively spliced isoforms and is encoded by a gene mapping to chromosome 12.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD27664-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD27664-25G
Lokale Artikelnummer::
BLDPBD27664-25G
Beschreibung:
1-(tert-Butoxycarbonyl)azetidine-2-carboxylic acid 95%
VE:
1 * 25 g
Artikel-Nr:
(BLDPBD54379-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD54379-100G
Lokale Artikelnummer::
BLDPBD54379-100G
Beschreibung:
1,4,9,12-Tetraoxadispiro[4.2.4.2]tetradecan 98%
VE:
1 * 100 g
Artikel-Nr:
(SCOI285221300)
Lieferant:
SI Analytics
Hersteller-Artikelnummer::
285221300
Lokale Artikelnummer::
SCOI285221300
Beschreibung:
Dieser photometrische Sensor kann wie jede andere Elektrode verwendet werden. Durch den USB- und den zusätzlichen analogen BNC/DIN-Anschluss kann er an jedem Titrator oder auch pH-Messgerät mit entsprechendem Messeingang angeschlossen werden. Die Stromversorgung erfolgt mit dem im Lieferumfang befindlichen USB-Hub, der über ein Netzteil verfügt.
VE:
1 * 1 ST
Lieferant:
Biotium
Beschreibung:
This antibody recognizes an oncofetal glycoprotein with a single chain of 70 kDa, which is identified as alpha fetoprotein (AFP). This MAb is highly specific to AFP and shows no cross-reaction with other oncofetal antigens or serum albumin. The yolk sac and the liver produce AFP during fetal life. AFP expression in adults is often associated with hepatoma or teratoma. However, hereditary persistence of alpha-fetoprotein may also be found in individuals with no obvious pathology. The protein is thought to be the fetal counterpart of serum albumin, and the AFP and albumin genes are present in tandem in the same transcriptional orientation on chromosome 4. AFP is found in monomeric as well as dimeric and trimeric forms, and binds copper, nickel, fatty acids and bilirubin. The level of AFP in amniotic fluid is used to measure renal loss of protein to screen for spinal bifida and anencephaly.
Artikel-Nr:
(SIAL200999-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
200999-5G
Lokale Artikelnummer::
SIAL200999-5G
Beschreibung:
12-Bromlaurinsäure, Sigma-Aldrich®
VE:
1 * 5 g
Lieferant:
WTW
Beschreibung:
Hochwertige, verbesserte Sensortechnologie kombiniert mit modernster Messelektronik. Die Elektroden verfügen über einen Steckkopf, der entweder mit einem IDS-Kabel oder mit einem Funkmodul verbunden werden kann.
Artikel-Nr:
(BOSSBS-12311R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12311R-FITC
Lokale Artikelnummer::
BOSSBS-12311R-FITC
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. The primary function of these motifs is to provide a versatile structural framework to mediate the formation of protein-protein interactions. LRRs are present in a variety of proteins with diverse structure and function, including innate immunity and nervous system development. Several human diseases are associated with mutations in genes encoding LRR-containing proteins. LRRC23 (leucine-rich repeat-containing protein 23), also known as leucine-rich protein B7, is a 343 amino acid protein that contains eight LRR (leucine-rich) repeasts and one LRRCT domain. LRRC23 exists as two alternatively spliced isoforms and is encoded by a gene mapping to chromosome 12.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12311R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12311R-A350
Lokale Artikelnummer::
BOSSBS-12311R-A350
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. The primary function of these motifs is to provide a versatile structural framework to mediate the formation of protein-protein interactions. LRRs are present in a variety of proteins with diverse structure and function, including innate immunity and nervous system development. Several human diseases are associated with mutations in genes encoding LRR-containing proteins. LRRC23 (leucine-rich repeat-containing protein 23), also known as leucine-rich protein B7, is a 343 amino acid protein that contains eight LRR (leucine-rich) repeasts and one LRRCT domain. LRRC23 exists as two alternatively spliced isoforms and is encoded by a gene mapping to chromosome 12.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13247R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13247R
Lokale Artikelnummer::
BOSSBS-13247R
Beschreibung:
Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (a photon, pheromone, odorant, hormone or neurotransmitter) while the effectors (i.e., adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein Alpha, Beta and Gamma polypeptides are encoded by at least 16, 4 and 7 genes, respectively. Most interest in G proteins has been focused on their Alpha subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Four distinct classes of G Alpha subunits have been identified; these include G Alpha s, G Alpha i, G Alpha q and G Alpha 12/13. The two members of the fourth class of G Alpha subunit proteins, G Alpha 12 and G Alpha 13, are insensitive to ADP-ribosylation by pertussis toxin, share 67% identity with each other and less than 45% identity with other G Alpha subunits and are widely expressed in a broad range of tissues.
VE:
1 * 100 µl
Lieferant:
3M
Beschreibung:
3M™ Solus™ Schutzbrille Serie 1000 mit starken Polycarbonat-Gläsern und einem schlanken, stilvollen Rahmen. Diese Brillen verfügen über eine Scotchgard™ Antibeschlag-/Antikratzbeschichtung sowie eine weiche Polsterung an Brillen- und Nasenbügel für zusätzlichen Tragekomfort.
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.
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.
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