Dynabeads™ M-280 Sheep IgG de antirrratón
Dynabeads™ M-280 Sheep IgG de antirrratón
Invitrogen™

Dynabeads™ M-280 Sheep IgG de antirrratón

El IgG antirratón de oveja Dynabeads M-280 son gránulos superparamagnéticos de 2,8 µm con IgG antirratón de oveja policlonal purificadoMás información
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Número de catálogoCantidad
11202D10 ml
11201D2 ml
Número de catálogo 11202D
Precio (USD)
-
Cantidad:
10 ml
El IgG antirratón de oveja Dynabeads M-280 son gránulos superparamagnéticos de 2,8 µm con IgG antirratón de oveja policlonal purificado covalentemente unido a superficie del gránulo. Estos gránulos están diseñados para admitir el enlace sencillo y eficaz de anticuerpos IgG de ratón y sus proteínas objetivo. Los Dynabeads uniformes, monodispersos y no porosas son la opción ideal para aplicaciones como la unión de Ig, la purificación de proteínas, inmunoensayos sándwich, la inmunoprecipitación (IP), la Co-IP y el aislamiento de células y microorganismos. El anticuerpo de oveja policlonal une IgG1, IgG2a, IgG2b de ratón y, con una menor reactividad, IgG3 e IgM de ratón. La reactividad cruzada humana es mínima.

• Aísle la proteína en menos de 40 minutos
• Enlaza con la mayoría de las subclases de IgG de ratón
• Unión no específica muy baja con alta relación señal-ruido
• Sin necesidad de columnas, centrifugaciones ni larga limpieza previa
• Alta reproducibilidad y alto rendimiento compatible con instrumentos KingFisher

La separación manual de Dynabeads es rápida y fácil de realizar
El anticuerpo primario que reconoce la molécula objetivo se puede añadir a la muestra (técnica indirecta) o usarse como revestimiento previo en el IgG antirratón de oveja Dynabeads M-280 (técnica directa). Independientemente de cuál de estas técnicas se utilicen, cuando los anticuerpos de oveja anti-IgG de ratón Dynabeads M-280 se mezcla con la muestra, los gránulos se enlazan con el objetivo. Al colocar la muestra en un imán DynaMag se separa el objetivo unido mediante gránulos del resto de la muestra. A continuación, se retira el sobrenadante mediante aspiración. La molécula diana se puede eluir de los gránulos con métodos de elución tradicionales o utilizar en aplicaciones como la inmunotransferencia (western blot) o espectrometría d masas, o en aplicaciones posteriores mientras sigue fijada a los gránulos.

La separación automatizada de Dynabeads ayuda a aumentar el rendimiento y reduce el tiempo de manipulación
Si está trabajando con varias muestras en paralelo, el número de pasos de lavado y el tiempo de manipulación aumenta proporcionalmente con el número de muestras. El pipeteo y otras manipulaciones manuales tienden a ser menos uniformes que la automatización cuando se trabaja con muchas muestras a la vez. Para manejar mejor un número de muestras de medio a alto rendimiento, reducir el tiempo de manipulación y asegurar una alta reproducibilidad, hemos desarrollado protocolos IP para los instrumentos KingFisher Flex y KingFisher Duo Prime. Los protocolos automatizados replican los protocolos manuales, que proporcionan un rendimiento proteico objetivo igual de alto y la misma unión no específica baja y alta reproducibilidad. No importa si está trabajando con 10 o 96 muestras, el protocolo IP es inferior a 40 minutos, independientemente. Solo tiene que cargar los reactivos en las placas, pulsar el botón de “inicio” y, para cuando haya preparado el análisis posterior, la IP estará lista. Es posible que sea necesaria cierta optimización (por ejemplo, los tiempos de incubación) dependiendo de su anticuerpo y de la abundancia y/o especificidad de su proteína objetivo.

• Utilice el instrumento Kingfisher Duo para un rendimiento de bajo a medio rendimiento (1-12 muestras/serie)
• Utilice el instrumento Kingfisher Flex para un alto rendimiento (12-96 muestras/serie)
Consulte los protocolos automatizados
Vea un vídeo sobre el instrumento Kingfisher Flex

Obtenga más información sobre Dynabeads
Consulte las guías de selección de inmunoprecipitación, los datos y las referencias
Consulte los imanes para las separaciones de Dynabeads
Buscar productos Dynabeads para otras aplicaciones

Compra de OEM
Para comprar IgG antirratón de oveja Dynabeads a nivel OEM, póngase en contacto con nuestro departamento de ventas de OEM y de Out-Licensing.

Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.

Especificaciones
Certificaciones/conformidadISO9001 and ISO13485
ColorBrown
Concentración10 mg/mL
DescripciónPolyclonal sheep anti-mouse IgG covalently bound to Dynabeads
Diámetro (métrico)2,8 μm
Para utilizar con (aplicación)Purificación de proteínas
Para utilizar con (equipo)Kingfisher™ Duo Prime, Kingfisher™ Flex, Kingfisher™ Apex, imanes DynaMag™
FormatoMicroesferas en suspensión
Compatibilidad de alto rendimientoCompatible con alto rendimiento
Tipo de ligandoAnticuerpo
MaterialPoliestireno
Cantidad10 ml
ReactividadUne IgG1, IgG2a e IgG2b de ratón. Reactividad más baja hacia IgG3 e IgM de ratón.
Estado normativoFor Research Use Only
Duración de almacenamiento36 meses a partir de la fecha de fabricación
Condiciones de envíoTemperatura ambiente
EspecieOveja
ObjetivoProteins
UniformidadMonosized 2.8 μm (CV <5%)
TipoIgG antirratón de oveja M-280
Unit SizeEach
Contenido y almacenamiento
Contiene: Anticuerpo de oveja anti-IgG de ratón Dynabeads™ M-280 de 10 mL (10 mg gránulos/mL)
Almacenamiento: 2 °C a 8 °C

Preguntas frecuentes

I am getting high background using Dynabeads M-280 Streptavidin magnetic beads. How can I prevent this from happening?

The background might be caused by nonspecific binding to the BSA on the bead surface. Alternatively, high background might be caused by nonspecific binding to streptavidin. Increasing either the pH or the salt concentration might help reduce the binding. Dynabeads M-270 Streptavidin magnetic beads might be a better alternative; these beads are not coated with BSA and are hydrophilic, as they are based upon carboxylic acid chemistry.

My Dynabeads magnetic beads are not pelleting well with the magnet. Do you have any suggestions for me?

Please review the following possibilities for why your Dynabeads magnetic beads are not pelleting:

- The solution is too viscous.
- The beads have formed aggregates because of protein-protein interaction.

Try these suggestions: - Increase separation time (leave tub on magnet for 2-5 minutes)
- Add DNase I to the lysate (~0.01 mg/mL)
- Increase the Tween 20 concentration to ~0.05% of the binding and/or washing buffer.
- Add up to 20 mM beta-merecaptoethanol to the binding and/or wash buffers.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

I have a long double-stranded DNA fragment I would like to isolate. What product do you recommend?

For biotin-labeled DNA that is less than 1 kb, we recommend you use Dynabeads M270 Streptavidin (Cat. No. 65305) and MyOne C1 magnetic beads (Cat. No. 65001). We recommend our Dynabeads KilobaseBINDER Kit (Cat. No. 60101), which is designed to immobilize long (>1 kb) double-stranded DNA molecules. The KilobaseBINDER reagent consists of M-280 Streptavidin-coupled Dynabeads magnetic beads along with a patented immobilization activator in the binding solution to bind to long, biotinylated DNA molecules for isolation. Please see the following link (https://www.thermofisher.com/us/en/home/life-science/dna-rna-purification-analysis/napamisc/capture-of-biotinylated-targets/immobilisation-of-long-biotinylated-dna-fragments.html) for more information in regards to long biotinylated DNA fragment isolation.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

Can I use Dynabeads magnetic beads to isolate single-stranded DNA templates?

Yes, Dynabeads magnetic beads can be used to isolate single-stranded DNA. Streptavidin Dynabeads magnetic beads can be used to target biotinylated DNA fragments, followed by denaturation of the double-stranded DNA and removal of the non-biotinylated strand. The streptavidin-coupled Dynabeads magnetic beads will not inhibit any enzymatic activity. This enables further handling and manipulation of the bead-bound DNA directly on the solid phase. Please see the following link (https://www.thermofisher.com/us/en/home/life-science/dna-rna-purification-analysis/napamisc/capture-of-biotinylated-targets/preparing-single-stranded-dna-templates.html) for more information in regards to single-stranded DNA capture.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

What is the magnetic susceptibility for Dynabeads magnetic beads?

Magnetic susceptibility is a measure of how quickly the beads will migrate to the magnet. This will depend on the iron content and the character of the iron oxide. The magnetic susceptibility given for the Dynabeads magnetic beads is the mass susceptibility, given either as cgs units/g or m^3/kg (the latter being an SI unit). For ferri- and ferromagnetic substances, the magnetic mass susceptibility is dependent upon the magnetic field strength (H), as the magnetization of such substances is not a linear function of H but approaches a saturation value with increasing field. For that reason, the magnetic mass susceptibility of the Dynabeads magnetic beads is determined by a standardized procedure under fixed conditions. The magnetic mass susceptibility given in our catalog is thus the SI unit. Conversion from Gaussian (cgs, emu) units into SI units for magnetic mass susceptibility is achieved by multiplying the Gaussian factor (emu/g or cgs/g) by 4 pi x 10^-3. The resulting unit is also called the rationalized magnetic mass susceptibility, which should be distinguished from the (SI) dimensionless magnetic susceptibility unit. In general, magnetic mass susceptibility is a measure of the force (Fz) influencing an object positioned in a nonhomogenous magnetic field. The magnetic mass susceptibility of the Dynabeads magnetic beads is measured by weighing a sample, and then subjecting the sample to a magnetic field of known strength. The weight (F1) is then measured, and compared to the weight of the sample when the magnetic field is turned off (F0). The susceptibility is then calculated as K x 10^-3 = [(F1-F0) x m x 0.335 x 10^6], where K is the mass susceptibility of the sample of mass m. The susceptibility is then converted to SI units.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

Citations & References (11)

Citations & References
Abstract
Development and mechanism of ?-secretase modulators for Alzheimer's disease.
Authors:Crump CJ, Johnson DS, Li YM
Journal:Biochemistry
PubMed ID:23614767
'?-Secretase is an aspartyl intramembranal protease composed of presenilin, Nicastrin, Aph1, and Pen2 with 19 transmembrane domains. ?-Secretase cleaves the amyloid precursor proteins (APP) to release Aß peptides that likely play a causative role in the pathogenesis of Alzheimer&#39;s disease (AD). In addition, ?-secretase cleaves Notch and other type I ... More
Characterization of the postsynaptic protein neurogranin in paired cerebrospinal fluid and plasma samples from Alzheimer's disease patients and healthy controls.
Authors:Kvartsberg H, Portelius E, Andreasson U, Brinkmalm G, Hellwig K, Lelental N, Kornhuber J, Hansson O, Minthon L, Spitzer P, Maler JM, Zetterberg H, Blennow K, Lewczuk P
Journal:
PubMed ID:26136856
'Synaptic dysfunction and degeneration are central events in Alzheimer''s disease (AD) pathophysiology that are thought to occur early in disease progression. Synaptic pathology may be studied by examining protein biomarkers specific for different synaptic elements. We recently showed that the dendritic protein neurogranin (Ng), including the endogenous Ng peptide 48 ... More
Brain amyloid-beta fragment signatures in pathological ageing and Alzheimer's disease by hybrid immunoprecipitation mass spectrometry.
Authors:Portelius E, Lashley T, Westerlund A, Persson R, Fox NC, Blennow K, Revesz T, Zetterberg H
Journal:
PubMed ID:25591542
'Senile plaques in Alzheimer''s disease (AD) are composed of amyloid-ß (Aß), especially N-truncated forms including Aß4-42. These are thought to be neurotoxic. However, individuals may live for decades with biomarker evidence of cerebral ß-amyloidosis (positive amyloid PET imaging and/or low cerebrospinal fluid levels of the 42 amino acid form of ... More
Pyroglutamate amyloid ß (Aß) aggravates behavioral deficits in transgenic amyloid mouse model for Alzheimer disease.
Authors:Wittnam JL, Portelius E, Zetterberg H, Gustavsson MK, Schilling S, Koch B, Demuth HU, Blennow K, Wirths O, Bayer TA
Journal:J Biol Chem
PubMed ID:22267726
'Pyroglutamate-modified Aß peptides at amino acid position three (Aß(pE3-42)) are gaining considerable attention as potential key players in the pathogenesis of Alzheimer disease (AD). Aß(pE3-42) is abundant in AD brain and has a high aggregation propensity, stability and cellular toxicity. The aim of the present work was to study the ... More
APP metabolism regulates tau proteostasis in human cerebral cortex neurons.
Authors:Moore S, Evans LD, Andersson T, Portelius E, Smith J, Dias TB, Saurat N, McGlade A, Kirwan P, Blennow K, Hardy J, Zetterberg H, Livesey FJ
Journal:
PubMed ID:25921538
'Accumulation of Aß peptide fragments of the APP protein and neurofibrillary tangles of the microtubule-associated protein tau are the cellular hallmarks of Alzheimer''s disease (AD). To investigate the relationship between APP metabolism and tau protein levels and phosphorylation, we studied human-stem-cell-derived forebrain neurons with genetic forms of AD, all of ... More