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P3555

Monoclonal Anti-Phosphothreonine antibody produced in mouse

clone PTR-8, ascites fluid

Oferta disponible

Sinónimos:

Monoclonal Anti-Phosphothreonine, Phospho Thr, Phospho Threonine, Phospho−Thr, Phospho-Threonine, p-Thr

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Talla/SKUDisponibilidadPrecio
100 μL
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482,00 €

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NACRES:
NA.44
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
PTR-8, monoclonal
Application:
ELISA (i), WB
Citations:
27

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biological source

mouse

Quality Segment

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

PTR-8, monoclonal

contains

15 mM sodium azide

technique(s)

indirect ELISA: 1:4,000, western blot: 1:50

isotype

IgG2b

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

General description

As determined by ELISA and dot blot, the antibody reacts specifically with phosphorylated threonine, both as free amino acid or conjugated to carriers such as BSA or KLH. No cross-reactivity is observed with non-phosphorylated threonine, phosphoserine, phosphotyrosine, AMP or ATP. This antibody has been used in immunoblotting for the localization of some phosphothreonine-containing proteins. Certain proteins known to contain phosphorylated threonine may not be recognized by this antibody due to steric hindrance of the recognition site.
Monoclonal Anti-Phosphothreonine (mouse IgG2b isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse.

Immunogen

phosphothreonine conjugated to keyhole limpet hemocyanin (KLH).

Application

Monoclonal Anti-Phosphothreonine antibody produced in mouse has been used in:immunoblotting, enzyme linked immuno sorbent assay (ELISA) ,dot blot.
Monoclonal and polyclonal antibodies directed against phosphorylated residues may be useful as analytical and preparative tools, by enabling the identification, quantification and immunoaffinity isolation of phosphorylated cellular proteins. Antibodies can be employed to monitor alterations in phosphorylation of specific proteins as they occur in intact organs or even whole animals.
Mouse monoclonal clone PTR-8 anti-phosphothreonine antibody may be used for the localization of phosphorylated threonine using various immunochemical assays such as ELISA, dot blot, and immunoblotting. Due to steric hindrance of the recognition site, this antibody may not recognize certain proteins known to contain phosphorylated threonine.
Mouse monoclonal clone PTR-8 anti-Phosphothreonine antibody reacts with phosphorylated threonine both as a free amino acid or when conjugated to carriers such as BSA or KLH, using ELISA and dot blot. It does not react with nonphosphorylated threonine, phosphorylated tyrosine or serine, AMP or ATP.

Biochem/physiol Actions

Protein phosphorylation and dephosphorylation are basic mechanisms for the modification of protein function in eukaryotic cells. Phosphorylation is a rare post-translational event in normal tissue. However, the abundance of phosphorylated cellular proteins increases tenfold following various activation processes, which are mediated through phosphotyrosine, phosphoserine or phosphothreonine (p-Tyr/p-Ser/p-Thr). Many different mitogenic systems, such as the EGF, PDGF and insulin receptor systems, contain Tyr/Ser/Thr kinase domains that autophosphorylate specific Tyr/Ser/Thr residues upon binding of their ligands. T cell antigen receptor complex or receptors for some hemopoietic growth factors may stimulate associated kinases, and cells transformed by viral oncogenes contain elevated levels of phosphorylated Tyr/Ser/Thr. An understanding of transformation by oncogenes and mitogenic processes of growth factors depends on the identification of their substrate and a subsequent determination of how phosphorylation affects the properties of these proteins.

Disclaimer

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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Este artículo
P6623P3430A1806
description

clone PTR-8, ascites fluid

description

clone PTR-8, purified from hybridoma cell culture

description

clone PSR-45, ascites fluid

description

clone PT-66, purified immunoglobulin, PBS solution

clone

PTR-8, monoclonal

clone

PTR-8, monoclonal

clone

PSR-45, monoclonal

clone

PT-66, monoclonal

antibody form

ascites fluid

antibody form

purified immunoglobulin

antibody form

ascites fluid

antibody form

purified immunoglobulin

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

agarose conjugate

technique(s)

indirect ELISA: 1:4,000, western blot: 1:50

technique(s)

indirect ELISA: 0.5-1 μg/mL, western blot: 5-10 μg/mL using A431 cell extracts, dot blot: suitable, immunoprecipitation (IP): suitable, microarray: suitable, immunocytochemistry: suitable

technique(s)

western blot: 1:500-1:1,000, indirect ELISA: 1:4,000

technique(s)

immunoprecipitation (IP): suitable

isotype

IgG2b

isotype

IgG2b

isotype

IgG1

isotype

IgG1


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Clase de almacenamiento

10 - Combustible liquids

¿Qué está pasando?

WGK 3

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable



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