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3,5-Difluor-4-methoxybenzonitril
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3,5-Difluor-4-methoxybenzonitril
Artikel-Nr:
(BOSSBS-4104R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4104R-HRP
Lokale Artikelnummer::
BOSSBS-4104R-HRP
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4104R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4104R-A680
Lokale Artikelnummer::
BOSSBS-4104R-A680
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5349R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5349R-A488
Lokale Artikelnummer::
BOSSBS-5349R-A488
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4104R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4104R-A647
Lokale Artikelnummer::
BOSSBS-4104R-A647
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
This antibody recognizes a protein of ~35 kDa, identified as CD74 (Workshop IV). CD74 is a type II transmembrane protein which binds to the peptide binding groove of newly synthesized MHC class II alpha/beta heterodimers and prevents their premature association with endogenous polypeptides. CD74 is expressed primarily by antigen presenting cells, such as B-lymphocytes (from before the pre-B cell stage to before the plasma cell stage), macrophages, and monocytes, and many epithelial cells. Anti-CD74 stains predominantly germinal center lymphocytes and B-cell lymphomas, but rarely T-cell lymphomas. Anti-CD74 has been shown to be useful in differentiating atypical fibroxanthoma (-) from malignant fibrous histiocytoma ( ).
Artikel-Nr:
(BOSSBS-8226R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-CY7
Lokale Artikelnummer::
BOSSBS-8226R-CY7
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Lieferant:
ABCR
Beschreibung:
Metal Beta-diketonates, Metal TMHD, Volatile Precursors for CVD
Lieferant:
COMBI-BLOCKS
Beschreibung:
1-Boc-3,5-dimethyl-1H-pyrazol-4-boronsäurepinakolester
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester 98%
Artikel-Nr:
(BOSSBS-8226R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-A350
Lokale Artikelnummer::
BOSSBS-8226R-A350
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD15550-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD15550-250MG
Lokale Artikelnummer::
BLDPBD15550-250MG
Beschreibung:
3-(Methoxycarbonyl)phenylboronsäurepinakolester 97%
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-8260R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R
Lokale Artikelnummer::
BOSSBS-8260R
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8409R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-CY5.5
Lokale Artikelnummer::
BOSSBS-8409R-CY5.5
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL225835-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
225835-5G
Lokale Artikelnummer::
SIAL225835-5G
Beschreibung:
Tris(6,6,7,7,8,8,8-heptafluor-2,2-dimethyl-3,5-octandionato-O,O')ytterbium(III), Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(611-3291)
Lieferant:
Sartorius Balances
Hersteller-Artikelnummer::
QUINTIX35-1S
Lokale Artikelnummer::
SARBQUINTIX35-1S
Beschreibung:
Eine Modellreihe von ergonomischen Waagen, konzipiert für eine einfache, intuitive Bedienung mit einem großen Touchscreen, selbsterklärenden Symbolen und einfachen Textaufforderungen. Zusätzlich zu den allgemeinen Wägeanwendungen, darunter allgemeines Wägen, Dichte, Prozentwägen, Kontrollwägen, Höchstwert, Zählen und Unruhewägen, bietet das Quintix® Sortiment auch die Funktionen Mischen, Komponenten, Statistiken und Umrechnen. Die Ergebnisse können über eine Mini-USB-Schnittstelle an einen Drucker oder einen Computer direkt in eine Microsoft Excel® Tabelle übertragen werden – ohne zusätzliche Software. Menüführung in 10 Sprachen.
VE:
1 * 1 ST
Artikel-Nr:
(K830-100ML)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRCK830-100ML
Beschreibung:
Gebrauchsfertiges, empfindliches Substrat für die Detektion von HRP (Meerrettichperoxidase)-Aktivität. Ideal für ELISA und Lösungsproben. Zeigt ein schnelleres Signal, gesteigerte Empfindlichkeit und geringstmöglichen Hintergrund.
VE:
1 * 100 mL
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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