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5-(3-Chlorophenyl)-3-hydroxypicolinic+acid
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5-(3-Chlorophenyl)-3-hydroxypicolinic+acid
Lieferant:
Thermo Scientific
Beschreibung:
1,1,1,3,3,3-Hexafluor-2-propanol 99% analysis_for
Artikel-Nr:
(BOSSBS-12497R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12497R-FITC
Lokale Artikelnummer::
BOSSBS-12497R-FITC
Beschreibung:
Apolipoproteins are protein components of plasma lipoproteins (1). The apolipoprotein C gene family encodes four homologous proteins designated apoC-I to -IV, which specifically modulate the metabolism of triglyceride-rich lipoproteins (2). The human apoC-I gene maps to chromosome 19q13.2 and is expressed primarily in the liver where it is activated when monocytes differentiate into macrophages (3,4). The human apoC-II gene maps to chromosome 19q13.2 and encodes a 79 amino acid single chain protein that is a necessary cofactor for the activation of lipoprotein lipase, the enzyme that hydrolyzes triglycerides in plasma and transfers the fatty acids to tissues (5–7). The human apoC-III gene maps to chromosome 11q23 and encodes a protein that may delay catabolism of triglyceride-rich particles by inhibiting lipoprotein lipase and hepatic lipase (8). The human apoC-IV gene maps to chromosome 19q13.2 and encodes a 127 amino acid protein that is primarily expressed in the liver (9,10).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8295R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8295R
Lokale Artikelnummer::
BOSSBS-8295R
Beschreibung:
Dipeptidyl peptidases (DPPs) mediate regulatory activity of their substrates and have been linked to a variety of diseases including type 2 diabetes, obesity and cancer. DPPs have post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. DPPs can bind specific voltage-gated potassium channels and alter their expression and biophysical properties and may also influence T cells. DPP proteins include DPRP1, DPRP2, DPP3, DPP7, DPP10, DPPX and CD26. DPRP1 (dipeptidyl-peptidase IV-related protein 1), also known as DPP8 (dipeptidyl-peptidase 8), DP8 or MSTP141, is a member of the peptidase S9B family of proteins that exhibit prolyl oligopeptidase activity. DPRP1 localizes to the cytoplasm and is ubiquitously expressed with predominant expression in placenta, brain, prostate, testis and muscle. DPRP1 is similar to CD26 (dipeptidyl peptidase IV) suggesting that it may be involved in immune function and participate in the activation of T-cells.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2408R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2408R-A647
Lokale Artikelnummer::
BOSSBS-2408R-A647
Beschreibung:
Class-IV neuronal intermediate filament that is able to self-assemble. It is involved in the morphogenesis of neurons. It may form an independent structural network without the involvement of other neurofilaments or it may cooperate with NF-L to form the filamentous backbone to which NF-M and NF-H attach to form the cross-bridges.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11780R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11780R-CY5
Lokale Artikelnummer::
BOSSBS-11780R-CY5
Beschreibung:
Nail-patella syndrome (NPS) is an autosomal dominant disorder characterized by dyplasia of finger nails, skeletal anomalies and, frequently, renal disease. NPS is caused by putative loss-of-function mutations in the transcription factor LMX1B. LMX1B belongs to the LIM-homeodomain family, members of which are known to be important for pattern formation during development. Twenty-two novel mutations may occur in the gene encoding LMX1B and the type and distribution of the mutations support the hypothesis that NPS is the result of haploinsufficiency for LMX1B. LMX1B is also necessary for normal development of the eye and in regulating dopaminergic neurogenesis and may be involved in developmental glaucoma and the aetiology of idiopathic Parkinson’s disease. Specifically, LMX1B along with LIM1 control the initial trajectory of motor axons in the developing mammalian limb. In addition, LMX1B directly regulates the coordinated expression of alpha 3(IV) and alpha 4(IV) collagen required for normal glomerular basement membrane (GBM) morphogenesis, and the dysregulation of LMX1B in GBM contributes to the renal pathology and nephrosis in NPS.
VE:
1 * 100 µl
Artikel-Nr:
(USBI123355)
Lieferant:
US Biological
Hersteller-Artikelnummer::
123355
Lokale Artikelnummer::
USBI123355
Beschreibung:
Anti-ANXA2 Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-2408R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2408R-A488
Lokale Artikelnummer::
BOSSBS-2408R-A488
Beschreibung:
Class-IV neuronal intermediate filament that is able to self-assemble. It is involved in the morphogenesis of neurons. It may form an independent structural network without the involvement of other neurofilaments or it may cooperate with NF-L to form the filamentous backbone to which NF-M and NF-H attach to form the cross-bridges.
VE:
1 * 100 µl
Lieferant:
OMEGA BIO-TEK
Beschreibung:
Das E.Z.N.A.® MicroElute Total RNA Kit bietet eine schnelle und einfache Methode zur Isolierung von bis zu 50 µg Gesamt-RNA aus kleinen Mengen an kultivierten eukaryotischen Zellen, Geweben wie lasergeschnittenen Proben (LDS) oder Feinnadelaspiraten (FNA). Normalerweise können bis zu 5×10⁵ eukaryotische Zellen oder 5 mg Gewebe in einem einzigen Experiment verwendet werden, je nach Art des Gewebes. Dieses Kit ermöglicht die Verarbeitung von einer oder mehreren Proben in weniger als 30 Minuten. Es sind keine Phenol-/Chloroformextraktionen und zeitaufwändige Arbeitsschritte wie die CsCl-Gradienten-Ultrazentrifugation erforderlich, und auch die Fällung mit Isopropanol oder LiCl entfällt. Aufgereinigte RNA kann mit 10 bis 15 µl nukleasefreiem Wasser eluiert werden. Die aufgereinigte RNA ist bereit für die meisten Folgeanwendungen wie RT-PCR, Northern Blotting, Poly A+ Aufreinigung, Nukleaseschutz und<i> In-vitro</i>-Translation.
Artikel-Nr:
(BOSSBS-11780R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11780R-A647
Lokale Artikelnummer::
BOSSBS-11780R-A647
Beschreibung:
Nail-patella syndrome (NPS) is an autosomal dominant disorder characterized by dyplasia of finger nails, skeletal anomalies and, frequently, renal disease. NPS is caused by putative loss-of-function mutations in the transcription factor LMX1B. LMX1B belongs to the LIM-homeodomain family, members of which are known to be important for pattern formation during development. Twenty-two novel mutations may occur in the gene encoding LMX1B and the type and distribution of the mutations support the hypothesis that NPS is the result of haploinsufficiency for LMX1B. LMX1B is also necessary for normal development of the eye and in regulating dopaminergic neurogenesis and may be involved in developmental glaucoma and the aetiology of idiopathic Parkinson’s disease. Specifically, LMX1B along with LIM1 control the initial trajectory of motor axons in the developing mammalian limb. In addition, LMX1B directly regulates the coordinated expression of alpha 3(IV) and alpha 4(IV) collagen required for normal glomerular basement membrane (GBM) morphogenesis, and the dysregulation of LMX1B in GBM contributes to the renal pathology and nephrosis in NPS.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11780R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11780R-A555
Lokale Artikelnummer::
BOSSBS-11780R-A555
Beschreibung:
Nail-patella syndrome (NPS) is an autosomal dominant disorder characterized by dyplasia of finger nails, skeletal anomalies and, frequently, renal disease. NPS is caused by putative loss-of-function mutations in the transcription factor LMX1B. LMX1B belongs to the LIM-homeodomain family, members of which are known to be important for pattern formation during development. Twenty-two novel mutations may occur in the gene encoding LMX1B and the type and distribution of the mutations support the hypothesis that NPS is the result of haploinsufficiency for LMX1B. LMX1B is also necessary for normal development of the eye and in regulating dopaminergic neurogenesis and may be involved in developmental glaucoma and the aetiology of idiopathic Parkinson’s disease. Specifically, LMX1B along with LIM1 control the initial trajectory of motor axons in the developing mammalian limb. In addition, LMX1B directly regulates the coordinated expression of alpha 3(IV) and alpha 4(IV) collagen required for normal glomerular basement membrane (GBM) morphogenesis, and the dysregulation of LMX1B in GBM contributes to the renal pathology and nephrosis in NPS.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11071R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11071R-A680
Lokale Artikelnummer::
BOSSBS-11071R-A680
Beschreibung:
This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10058R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10058R-A555
Lokale Artikelnummer::
BOSSBS-10058R-A555
Beschreibung:
Endopeptidase that degrades various components of the extracellular matrix, such as aggrecan and cartilage oligomeric matrix protein (comp), during development, haemostasis and pathological conditions (arthritic disease). May also play a role in neovascularization or angiogenesis. Hydrolyzes collagen type IV, laminin, nidogen, nascin-C isoform, fibronectin, and type I gelatin.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8116R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8116R-CY7
Lokale Artikelnummer::
BOSSBS-8116R-CY7
Beschreibung:
Component of some MITRAC complex, a cytochrome c oxidase (COX) assembly intermediate complex that regulates COX assembly. MITRAC complexes regulate both translation of mitochondrial encoded components and assembly of nuclear-encoded components imported in mitochondrion. Required for efficient translation of MT-CO1 and mitochondrial respiratory chain complex IV assembly.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11071R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11071R-CY5
Lokale Artikelnummer::
BOSSBS-11071R-CY5
Beschreibung:
This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6728R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6728R-CY5.5
Lokale Artikelnummer::
BOSSBS-6728R-CY5.5
Beschreibung:
Ca2+/calmodulin dependent protein kinase type IV (CAMKIV) belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. This enzyme is a multifunctional serine/threonine protein kinase with limited tissue distribution, that has been implicated in transcriptional regulation in lymphocytes, neurons and male germ cells.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4226R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4226R-A647
Lokale Artikelnummer::
BOSSBS-4226R-A647
Beschreibung:
VAPA is a type IV membrane protein, present in the plasma membrane, intracellular vesicles and may also be associated with the cytoskeleton. This protein may function in vesicle trafficking, membrane fusion, protein complex assembly and cell motility. Two transcript variants encoding distinct isoforms have been identified.
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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