Partículas magnéticas de proteína A/G de grado ChIP Pierce™
Partículas magnéticas de proteína A/G de grado ChIP Pierce™
Thermo Scientific™

Partículas magnéticas de proteína A/G de grado ChIP Pierce™

Gránulos de polímero recubiertos de magnetita y proteína a 10 mg/ml en agua con azida sódica. Suficiente para: Uso enMás información
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Número de catálogoCantidad
261625 mL
Número de catálogo 26162
Precio (USD)
1.668,60
Each
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Cantidad:
5 mL
Pedido a granel o personalizado
Precio (USD)
1.668,60
Each
Añadir al carro de la compra
Gránulos de polímero recubiertos de magnetita y proteína a 10 mg/ml en agua con azida sódica. Suficiente para: Uso en aproximadamente 250 ensayos de ChIP típicos

Más datos del producto
Análisis de la regulación de la actividad transcripcional dependiente de andrógenos e independiente

Productos relacionados
Proteína A/G Plus Agarosa Pierce™ grado ChIP
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
DescripciónPierce ChIP-grade Protein A/G Magnetic Beads
Tipo de ligandoProteína A/G
Cantidad5 mL
Suficiente paraAprox. 250 ensayos
ObjetivoAnticuerpo
Línea de productosPierce
TipoGránulo magnético
Unit SizeEach
Contenido y almacenamiento
Se debe almacenar en un recipiente original protegido de la luz solar directa en una zona seca, fresca y bien ventilada.

Preguntas frecuentes

What are the differences between Protein A, Protein G, Protein A/G, and Protein L Ig-binding proteins?

Protein A, Protein G, and Protein A/G bind almost exclusively to the IgG class of antibodies, but their binding properties differ among species and subclasses of IgG. Protein L binds in the variable fragment of some kappa light chains and can react with any immunoglobulin, not just IgG, as long as the correct kappa light chains are present. Protein L does not bind lambda light chains and certain kappa chains of different species.

-Protein A is generally preferred for rabbit, pig, dog, and cat IgG.
-Protein G has better binding capacity for a broader range of mouse and human IgG subclasses (e.g., IgG1 vs. IgG2)
-Protein A/G is a recombinant fusion protein that includes the IgG-binding domains of both Protein A and Protein G. Therefore, Protein A/G is ideal for binding the broadest range of IgG subclasses from rabbit, mouse, human, and other mammalian samples.
-Protein L binds to certain immunoglobulin kappa light chains. Because kappa light chains occur in members of all classes of immunoglobulin (i.e., IgG, IgM, IgA, IgE and IgD), Protein L can purify these different classes of antibody. However, only those antibodies within each class that possess the appropriate kappa light chains will bind. Generally, empirical testing is required to determine if Protein L is effective for purifying a particular antibody. It binds only Vk1 in mouse and VkI, VkIII and VkIV in human.
Read more about the general characteristics of Ig-binding proteins (https://www.thermofisher.com/us/en/home/life-science/antibodies/antibody-purification-kits-reagents.html) and (https://assets.thermofisher.com/TFS-Assets/LSG/Application-Notes/TR0034-Ab-binding-proteins.pdf).

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Citations & References (4)

Citations & References
Abstract
CTCF loss mediates unique DNA hypermethylation landscapes in human cancers
Authors:Nathan A. Damaschke, Joseph Gawdzik, Mele Avilla, Bing Yang, John Svaren, Avtar Roopra, Jian-Hua Luo, Yan P. Yu, Sunduz Keles & David F. Jarrard
Journal:Clinical Epigenetics
PubMed ID:
MiR-4319 hinders YAP expression to restrain non-small cell lung cancer growth through regulation of LIN28-mediated RFX5 stability
Authors:Yi Yang, He Li, Yu Liu, Chuang Chi, Jiangwei Ni, Xiaoming Lin
Journal:Biomedicine & Pharmacotherapy
PubMed ID:
Identification of Cancer Drivers at CTCF Insulators in 1,962 Whole Genomes
Authors:Liu et al.
Journal:Cell Systems
PubMed ID:
Targeting WD repeat domain 5 enhances chemosensitivity and inhibits proliferation and programmed death-ligand 1 expression in bladder cancer
Authors:Zhang J, Zhou Q, Xie K, Cheng L, Peng S, Xie R, Liu L, Zhang Y, Dong W, Han J, Huang M, Chen Y, Lin T, Huang J, Chen X
Journal: Exper Clin Cancer Res
PubMed ID: