Ugrás a tartalomra
Merck

P5872

Sigma-Aldrich

Anti-Phosphotyrosine antibody, Mouse monoclonal

clone PT-66, purified from hybridoma cell culture

Szinonimák:

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

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
NACRES:
NA.44
konjugátum:
unconjugated
application:
ELISA (i)
FACS
ICC
IHC
IP
RIA
WB
klón:
PT-66, monoclonal
technika/technikák:
flow cytometry: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
indirect ELISA: 0.5-1.0 μg/mL using phosphotyrosine conjugated to BSA
radioimmunoassay: suitable
western blot: 0.25-0.5 μg/mL using total cell extract of human platelets
citations:
17

biológiai forrás

mouse

Minőségi szint

konjugátum

unconjugated

antitest forma

purified immunoglobulin

antitest terméktípus

primary antibodies

klón

PT-66, monoclonal

Forma

buffered aqueous solution

kiszerelés

antibody small pack of 25 μL

koncentráció

~2 mg/mL

technika/technikák

flow cytometry: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
indirect ELISA: 0.5-1.0 μg/mL using phosphotyrosine conjugated to BSA
radioimmunoassay: suitable
western blot: 0.25-0.5 μg/mL using total cell extract of human platelets

izotípus

IgG1

kiszállítva

dry ice

tárolási hőmérséklet

−20°C

célzott transzláció utáni módosítás

unmodified

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Általános leírás

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 PT-66 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with phosphotyrosine-BSA conjugate.

Egyediség

Monoclonal Anti-Phosphotyrosine is specific for phosphorylated tyrosine both as the free amino acid or when conjugated to carriers such as BSA or KLH. It does not react with non-phosphorylated tyrosine or other phosphorylated amino acids, including serine

Immunogén

phosphotyrosine conjugated to BSA

Alkalmazás

Monoclonal Anti-Phosphotyrosine has been used in
  • immunoblotting,
  • immunofluorescence,
  • immunohistochemistry
  • immunocytochemistry
  • flow cytometry
  • immunoprecipitation
  • enzyme linked immunosorbent assay (ELISA)
  • radio immunoassay (RIA)
  • immunoaffinity isolation

Biokémiai/fiziológiai hatások

Protein phosphorylation is a basic signaling mechanism that modifies protein function in eukaryotic cells. Serine, threonine, and tyrosine are the major phosphorylated amino acids in proteins. Tyrosine phosphorylation is a rare post-translational event in normal tissues, accounting for only 0.03% of phosphorylated amino acids. However, this phosphorylation increases several folds by various activation signals and the process is mediated by protein tyrosine kinases. Protein-tyrosine kinases (PTKs) are enzymes that catalyze the transfer of γ-phosphate of ATP to tyrosine residues of protein substrates. The PTKs are responsible for many biological processes like cell cycle, proliferation, oncogenesis, and development.

Fizikai forma

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

Jogi nyilatkozat

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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Tárolási osztály kódja

12 - Non Combustible Liquids

WGK

WGK 2

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


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Analitikai tanúsítványok (COA)

Lot/Batch Number

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Neumeister P, et al.
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Lymphatic vessels function to drain interstitial fluid from a variety of tissues. Although shear stress generated by fluid flow is known to trigger lymphatic expansion and remodeling, the molecular basis underlying flow-induced lymphatic growth is unknown. We aimed to gain
Amy M Nichols et al.
Methods in molecular biology (Clifton, N.J.), 492, 143-160 (2009-02-26)
Mass spectrometry-based analysis of protein phosphorylation has become increasingly powerful over the past decade and has been applied to many different biological systems. One of the most significant concerns facing the phosphoproteomics community and the proteomics field as a whole
alpha1 Integrin cytoplasmic domain is involved in focal adhesion formation via association with intracellular proteins
LOSTER K, et al.
The Biochemical Journal, 356(1), 233-240 (2001)
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Shah MA, et al.
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