G9545
Anti-GAPDH antibody produced in rabbit
~1 mg/mL, affinity isolated antibody, buffered aqueous solution
Sinónimos:
Anti-G3PD, Anti-GAPD, Anti-OCAS, Anti-coactivador OCT1 en fase S, Anti-gliceraldehído-3-fosfato deshidrogenasa, Componente anti-38-kD, Componente anti-p38
About This Item
Productos recomendados
biological source
rabbit
Quality Level
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen ~36 kDa
species reactivity
mouse, rat, human
concentration
~1 mg/mL
technique(s)
immunoprecipitation (IP): 5-10 μg using mouse NIH3T3 cell lysates
indirect immunofluorescence: 5-10 μg/mL using rat NRK cells
western blot: 0.1-0.2 μg/mL using whole extract of human HeLa cells
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... GAPDH(2597)
mouse ... Gapdh(14433)
rat ... Gapdh(24383)
General description
Specificity
Immunogen
Application
- extracto de células cancerosas humanas
- extracto de tejido muscular de ratones añosos con sarcopenia
- trabéculas o muestras del miocardio del corazón de ratones
- fibroblastos embrionarios de ratón
Biochem/physiol Actions
Physical form
Storage and Stability
Para una conservación prolongada, congelar en alícuotas de trabajo. No se recomienda la congelación y descongelación repetidas o la conservación en congeladores “frost free”. Si aparece una turbidez ligera tras una conservación prolongada, clarifique la disolución centrifugándola antes de usarla. Las diluciones de trabajo deben desecharse si no se utilizan en 12 horas.
Disclaimer
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Storage Class
10 - Combustible liquids
wgk_germany
WGK 1
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Certificados de análisis (COA)
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Artículos
The field of proteomics is continually looking for new ways to investigate protein dynamics within complex biological samples. Recently, many researchers have begun to use RNA interference (RNAi) as a method of manipulating protein levels within their samples, but the ability to accurately determine these protein amounts remains a challenge. Fortunately, over the past decade, the field of proteomics has witnessed significant advances in the area of mass spectrometry. These advances, both in instrumentation and methodology, are providing researchers with sensitive assays for both identification and quantification of proteins within complex samples. This discussion will highlight some of these methodologies, namely the use of Multiple Reaction Monitoring (MRM) and Protein-AQUA.
Loading controls in western blotting application.
We presents an article about the Warburg effect, and how it is the enhanced conversion of glucose to lactate observed in tumor cells, even in the presence of normal levels of oxygen. Otto Heinrich Warburg demonstrated in 1924 that cancer cells show an increased dependence on glycolysis to meet their energy needs, regardless of whether they were well-oxygenated or not.
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