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Potassium+hexacyanocobaltate(III)
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Potassium+hexacyanocobaltate(III)
Artikel-Nr:
(BOSSBS-5144R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5144R-CY5
Lokale Artikelnummer::
BOSSBS-5144R-CY5
Beschreibung:
This gene is a member of the natriuretic peptide family and encodes a secreted protein which functions as a cardiac hormone. The protein undergoes two cleavage events, one within the cell and a second after secretion into the blood. The protein's biological actions include natriuresis, diuresis, vasorelaxation, inhibition of renin and aldosterone secretion, and a key role in cardiovascular homeostasis. A high concentration of this protein in the bloodstream is indicative of heart failure. Mutations in this gene have been associated with postmenopausal osteoporosis. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR12045-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR12045-1G
Lokale Artikelnummer::
APOSOR12045-1G
Beschreibung:
3-(4-Bromo-3-methylphenyl)-2-thioxo-2,3-dihydro-4(1H)-quinazolinone
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-(4-Bromophenyl)-5-methyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone
Artikel-Nr:
(BOSSBS-11267R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11267R-HRP
Lokale Artikelnummer::
BOSSBS-11267R-HRP
Beschreibung:
CCT2 is one of eight largely unrelated subunit proteins found in a protein chaperone complex known as the chaperonin-containing TCP-1 (CCT) or TRiC complex. The CCT complex is an abundanct cytoslic component that is credited with helping newly synthesized polypeptides adopt the correct conformation (1). Proteins that fold and assemble with the help of CCT include the cytoskeletal proteins actin and tubulin as well as up to 15% of newly synthesized eukaryotic proteins (2). CCT2 is the β-subunit of the chaperone complex and is one of several CCT proteins that exhibit increased expression in response to stress. This implies that the CCT complex helps cells recover from protein damage by assisting in protein folding and assembly (3). CCT subunit levels also change throughout the cell cycle, with lower proteins levels (and reduced chaperone activity) found during induced cell cycle arrest during at M phase (4). Each CCT subunit is thought to perform a specific function during protein folding and assembly (5); CCT2 exhibits both actin and tubulin binding activities (6,3) but the exact molecular function on this subunit remains uncertain.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4183R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4183R-A488
Lokale Artikelnummer::
BOSSBS-4183R-A488
Beschreibung:
Rabphilin-3AL (rabphilin-3A-like), also known as RPH3AL or NOC2, is a cytoplasmic Rab GTPase effector. It contains one FYVE-type zinc finger and one Rab-binding (RBD) domain, but unlike its related protein, rabphilin-3A, rabphilin-3AL does not contain any C2 domains. Rabphilin-3AL is expressed in a variety of tissues, with highest levels found in kidney, skeletal muscle, pancreas, liver, ovary, stomach, heart and thyroid. It is believed to play a role regulating calcium-dependent secretory vesicle exocytosis in endocrine and exocrine cells. Via its RBD domain, rabphilin-3AL is capable of binding Rab 27a and, through this interaction, rabphilin-3AL is recruited to dense-core vesicles. With lower affinity, rabphilin-3AL can also bind Rab 3 and Rab 8 with its RBD domain. Through an interaction with Rab 3, rabphilin-3AL can inhibit G-protein signaling in endocrine pancreas and positively regulate insulin secretion. Rabphilin-3AL knockout mice display accumulation of secretory granules and irregular shape in exocrine cells.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Acetyl-6-tert-butyl-1,1-dimethylindan
Artikel-Nr:
(APOSOR18001-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR18001-1G
Lokale Artikelnummer::
APOSOR18001-1G
Beschreibung:
2-(1,3-Benzoxazol-2-yl)-1-(4-tert-butylphenyl)ethanone 95+%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Bromo-5-(trifluoromethyl)pyridin-2-ol 98%
Artikel-Nr:
(BOSSBS-9135R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9135R-A488
Lokale Artikelnummer::
BOSSBS-9135R-A488
Beschreibung:
Members of the suppressor of cytokine signaling (SOCS) family of proteins contain C-terminal regions of homology called the SOCS box, which serves to couple SOCS proteins and their binding partners with the Elongin B and C complex. Several other families of proteins also contain SOCS boxes, but differ from the SOCS proteins in the type of domain they contain upstream of the SOCS box. The largest family of SOCS box-containing proteins is the ankyrin repeat and SOCS box-containing (ASB) protein family. Members of the ASB family include ASB-1 through ASB-18 and are involved in a variety of biological processes. ASB-17 is a 295 amino acid member of this family. ASB-17 contains one ankyrin repeat and one SOCS box domain. ASB-17 is thought to be a substrate-recognition subunit of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin protein ligase complex. This complex mediates the ubiquitination of target proteins and their subsequent proteasomal degradation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9135R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9135R-A350
Lokale Artikelnummer::
BOSSBS-9135R-A350
Beschreibung:
Members of the suppressor of cytokine signaling (SOCS) family of proteins contain C-terminal regions of homology called the SOCS box, which serves to couple SOCS proteins and their binding partners with the Elongin B and C complex. Several other families of proteins also contain SOCS boxes, but differ from the SOCS proteins in the type of domain they contain upstream of the SOCS box. The largest family of SOCS box-containing proteins is the ankyrin repeat and SOCS box-containing (ASB) protein family. Members of the ASB family include ASB-1 through ASB-18 and are involved in a variety of biological processes. ASB-17 is a 295 amino acid member of this family. ASB-17 contains one ankyrin repeat and one SOCS box domain. ASB-17 is thought to be a substrate-recognition subunit of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin protein ligase complex. This complex mediates the ubiquitination of target proteins and their subsequent proteasomal degradation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8480R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8480R-A488
Lokale Artikelnummer::
BOSSBS-8480R-A488
Beschreibung:
RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions that affect males more frequently as males carry a single X chromosome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13475R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13475R-A488
Lokale Artikelnummer::
BOSSBS-13475R-A488
Beschreibung:
Glucosamine 6-phosphate N-acetyltransferase (GNA1), also designated phosphoglucosamine transacetylase or phosphoglucosamine acetylase, belongs to the GNA1 subfamily of the larger acetyltransferase family of proteins. GNA1, a peripheral membrane protein containing one N-acetyltransferase domain, is expressed in the colon and maps to cytoband 14q22.1. The protein localizes to the Golgi apparatus and the endosome. It is important for UDP-GlcNAc biosynthesis pathway. GNA1 catalyzes the synthesis of GlcNAc6P from AcCoA and GlcN6P, a step in the UDP-GlcNAc6P formation pathway.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
Das AccuBlue® NextGen dsDNA-Quantifizierungs-Kit bietet ein unvergleichliches Maß an Sensitivität in der dsDNA-Detektion. Es stellt eine sensitive und präzise Methode zur DNA-Quantifizierung für geringste Mengen von DNA dar, mit einer Nachweisgrenze von nur einem pg DNA in einem 96-Well-Mikrotiterplatten-Reader-Assay.
Lieferant:
ENTEGRIS
Beschreibung:
Die sichere und bequeme Methode zur Verbindung von wiederverwendbaren FluoroPure®-Chemikalienbehältern mit Großmengenabgabesystemen. Das patentierte Design Keycode, um ein unsicheres Mischen von Chemikalien zu verhindern und gleichzeitig einen engagierten sauberen Service zu gewährleisten. Ein Anschluss ermöglicht die Abgabe, Entlüftung und Füllstandserkennung.
Artikel-Nr:
(BOSSBS-0235R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0235R-CY3
Lokale Artikelnummer::
BOSSBS-0235R-CY3
Beschreibung:
PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0235R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0235R-CY5
Lokale Artikelnummer::
BOSSBS-0235R-CY5
Beschreibung:
PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
VE:
1 * 100 µl
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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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