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A1806

Sigma-Aldrich

Monoclonal Anti-Phosphotyrosine−Agarose antibody produced in mouse

clone PT-66, purified immunoglobulin, PBS solution

Sinônimo(s):

Monoclonal Anti-Phosphotyrosine, Phospho-Tyr, Phospho-tyrosine, p-Tyr

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.44

fonte biológica

mouse

Nível de qualidade

recombinante

expressed in mouse cell line

conjugado

agarose conjugate

forma do anticorpo

purified immunoglobulin

tipo de produto de anticorpo

primary antibodies

clone

PT-66, monoclonal

Formulário

PBS solution

técnica(s)

immunoprecipitation (IP): suitable

Isotipo

IgG1

capacidade

1 mg/mL binding capacity

Condições de expedição

wet ice

temperatura de armazenamento

2-8°C

modificação pós-traducional do alvo

phosphorylation (pTyr)

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Descrição geral

As determined by ELISA and competitive ELISA, the antibody reacts specifically with phosphorylated tyrosine, both as free amino acid or conjugated to carriers such as BSA or KLH. No cross-reactivity is observed with non-phosphorylated tyrosine, phosphothreonine, phosphoserine, AMP or ATP.
Monoclonal Anti-Phosphotyrosine (mouse IgG1 isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse.

Imunogênio

phosphotyrosine conjugated to BSA

Aplicação

Monoclonal Anti-Phosphotyrosine-Agarose antibody produced in mouse has been used in:
  • immunoprecipitation experiments for affinity-purification of phosphotyrosine proteins
  • phosphotyrosine pulldown assays
  • PI3-kinase assay

Proteins containing phosphotyrosines were deteced in protein extracts from dissected tissue of Harlan Sprague Dawley rats or from transfected HEK293 cells using mouse monoclonal anti-phosphotyrosine antibody as the primary antibody. Reactivity was blocked when extracts were previously treated with 10 mM phosphotyrosine but not 10 mM tyrosine showing the specifity of the antibody for phosphorylated tyrosines. Immunoprecipitation of proteins containing phosphorylated tyrosines in rat dorsat root ganglion homogenates was performed using mouse monoclonal anti-phosphotyrosine. The antibody was incubated with the homogenates in the presence of 50 mm NaF and protease inhibitors for 4-14 hours at 4°. The antibody was precipitated using Protein G-agarose beads incubated overnight.

Ações bioquímicas/fisiológicas

Reversible phosphorylation of proteins is an important post-translational modification that plays a regulatory role in the expression of most proteins in the cells. Reversible phosphorylation at multiple serine, tyrosine and threonine residues mediate numerous signalling pathways in both prokaryotic and Eukaryotic cells. Cellular proteins with phosphorylated tyrosine increase many fold by the activation of tyrosine kinases. Most mitogenic receptor systems such as EGF, PDGF, insulin receptors contain tyrosine kinase domains that undergo autophosphorylation when receptors bind to the respective ligands. Tyrosine-specific protein kinase activity has also been described in many retroviral oncogene proteins. Cells transformed by these oncogenes contain elevated levels of phosphotyrosine. Many of the oncogenes found in mammalian oncogenic viruses encode tyrosine protein kinases that reside in the cellular cytoplasm. Others encode transmembrane receptors whose tyrosine phosphotransferase activity is stimulated by the binding of ligand to the extracellular domain.

forma física

Suspension in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide

Exoneração de responsabilidade

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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J A Houmard et al.
The American journal of physiology, 277(6 Pt 1), E1055-E1060 (1999-12-22)
The purpose of this study was to determine if the improvement in insulin sensitivity with exercise training is associated with enhanced phosphatidylinositol 3-kinase (PI 3-kinase) activity. Nine sedentary men were studied before and after 7 days of exercise training (1
M S Hickey et al.
Journal of applied physiology (Bethesda, Md. : 1985), 83(3), 718-722 (1997-09-18)
The purpose of this investigation was to determine whether insulin-stimulated phosphatidylinositol 3-kinase (PI3-kinase) activity is detectable in needle biopsies of human skeletal muscle. Sixteen healthy nonobese males matched for age, percent fat, fasting insulin, and fasting glucose participated in one
Insulin activation of phosphatidylinositol 3-kinase in human skeletal muscle in vivo
Hickey MS, et al.
Journal of Applied Physiology, 83(3), 718-722 (1997)
Tyrosine 116 of the herpes simplex virus type 1 IE alpha 22 protein is an ocular virulence determinant and potential phosphorylation site
Brandt CR and Kolb AW
Investigative Ophthalmology & Visual Science, 44(11), 4601-4607 (2003)
RET oncoproteins induce tyrosine phosphorylation changes of proteins involved in RNA metabolism
Gorla L, et al.
Cellular Signalling, 18(12), 2272-2282 (2006)

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