S7273
Sera from mouse
frozen liquid (from clotted whole blood)
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About This Item
Productos recomendados
origen biológico
mouse
Nivel de calidad
descripción
Contains no azides
esterilidad
sterile; aseptically filled
formulario
frozen liquid (from clotted whole blood)
origen
USA origin
Condiciones de envío
dry ice
temp. de almacenamiento
−20°C
Categorías relacionadas
Descripción general
Mouse serum is used in a variety of mouse cell culture systems to study viral infection, inhibition, and transduction processes.
Aplicación
Sera from mouse has been used:
- as a source of inter-α-inhibitor (IαI) in protein modification to form the heavy chain (HC)-hyaluronan (HA) complex
- to culture primary mouse airway smooth muscle cells (MASM) and primary human airway smooth muscle cells (HASM)
- as analytical quality control (QC) sample for metabolomics analysis of treated mice serum
Idoneidad
Not tested for use in cell culture
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves
Certificados de análisis (COA)
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The Journal of biological chemistry, 288(1), 205-214 (2012-11-21)
The covalent transfer of heavy chains (HCs) from inter-α-inhibitor (IαI) to hyaluronan (HA) via the protein product of tumor necrosis factor-stimulated gene-6 (TSG-6) forms the HC-HA complex, a pathological form of HA that promotes the adhesion of leukocytes to HA
Nature microbiology, 1(11), 16140-16140 (2016-10-27)
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The Journal of biological chemistry, 284(8), 5313-5323 (2008-12-17)
The covalent association of inter-alpha-inhibitor-derived heavy chains (HCs) with hyaluronan was first described in synovial fluid from arthritic patients and later described as a structural and functional component of hyaluronan "cable" structures produced by many different cells and stimuli. HC
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Adeno-associated virus (AAV)-based vectors are promising gene delivery vehicles for human gene transfer. One significant obstacle to AAV-based gene therapy is the high prevalence of neutralizing antibodies in humans. Until now, it was thought that, except for nonhuman primates, pre-existing
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