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Merck
CN

05-1000

Anti-Phosphoserine Antibody, clone 4A4 (mouse IgG1)

clone 4A4, Upstate®, from mouse

Synonym(s):

Clone 4A4 Anti-Phosphoserine, Phosphoserine Detection Antibody

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
4A4, monoclonal
Species reactivity:
vertebrates
Application:
ELISA, FACS, IF, IHC, WB
Citations:
31
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biological source

mouse

Quality Level

antibody form

purified antibody

antibody product type

primary antibodies

clone

4A4, monoclonal

species reactivity

vertebrates

manufacturer/tradename

Upstate®

technique(s)

ELISA: suitable, flow cytometry: suitable, immunofluorescence: suitable, immunohistochemistry: suitable (paraffin), western blot: suitable

isotype

IgG1

shipped in

dry ice

target post-translational modification

phosphorylation (pSer)

General description

Dependent upon the molecular weight of the serine phosphorylated protein being detected.
The identification of protein phosphorylation as a regulatory mechanism originated from studies by Fischer and Krebs in the mid 1950s that later earned them the 1992 Nobel prize. It is the major mechanism for the regulation of diverse cellular processes including cell division, protein synthesis, transcriptional regulation and neurotransmission. The steady state phosphorylation of any given substrate is governed by the opposing activities of kinases and phosphatases. It is now believed that a third of all eukaryotic cellular proteins are phosphorylated and that the majority of all phosphorylation events occur on serine and threonine residues (>95%).

Immunogen

Phosphoserine coupled to KLH.

Application

Detect Phosphoserine using this Anti-Phosphoserine Antibody, clone 4A4 (mouse IgG1) validated for use in ELISA, FC, IF, IH(P) & WB.
Immunofluorescence

Flow Cytometry

Immunohistochemistry (Paraffin)

ELISA
Research Category
Signaling
Research Sub Category
General Post-translation Modification

Biochem/physiol Actions

This antibody recognizes serine-phosphorylated proteins from all species.

Physical form

Format: Purified
Protein G-Sepharose Chromatography
Purified mouse monoclonal IgG1 in buffer containing PBS with 0.1% sodium azide and 30% glycerol.

Preparation Note

Stable for 1 year at -20ºC from date of receipt.
For maximum recovery, centrifuge the original vial prior to cap removal. If the product has accidentally been frozen and thawed, spin it at 13,000 x g for 10 minutes at 2-8°C.

Analysis Note

Routinely evaluated by Western Blot analysis on lysate from Calyculin A/Okadaic-treated human A431 carcinoma cells.

Western Blot Analysis:
0.5–2 μg/mL of this lot detected serinephosphorylated proteins in a lysate from either insulin or Calyculin A/Okadaic-treated human A431 carcinoma cells.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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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wgk

WGK 2

Storage Class

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Articles

蛋白磷酸化是一种可逆的翻译后加工,在细胞内信号传递中有非常重要的功能。采用Western Blotting技术检测磷酸化蛋白是探讨信号传导中上游调控、下游功能调整、信息交流及反馈机制等的基本手段。我们提供专用的优质试剂和研究方法,帮助你获得准确、灵敏的磷酸化检测数据。


Nucleocytoplasmic shuttling of a GATA transcription factor functions as a development timer.
Cai, H; Katoh-Kurasawa, M; Muramoto, T; Santhanam, B; Long, Y; Li, L; Ueda, M; Iglesias et al.
Science (New York, N.Y.) null
Peng Wang et al.
Carcinogenesis, 32(2), 146-153 (2010-11-04)
It is well established that the tumorigenic potential of nucleophosmin (NPM)-anaplastic lymphoma kinase (ALK), an oncogenic tyrosine kinase, is dependent on its tyrosine phosphorylation. Using tandem affinity purification-mass spectrometry, we found evidence of phosphorylation of three serine residues of NPM-ALK
Glycine receptor internalization by protein kinases activation.
Miguel Angel Velazquez-Flores,Rocio Salceda,Miguel ??ngel Vel?!zquez-Flores,Roc?-o Salceda
Synapse null



Global Trade Item Number

SKUGTIN
47640-U04061838110473