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Phosphoserine Monoclonal Antibody

Phosphoserine Monoclonal Antibody

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Specification

Product name Phosphoserine Monoclonal Antibody
Immunogen Purified Protein
Host Mouse
Reactivity All
Applications IHC-P, WB
Applications notes Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:1000-1:2000).
Clonality Monoclonal
Preparation method The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen

Product Properties

Formulation Liquid solution
Concentration 1 mg/ml
Storage buffer PBS, pH 7.4, containing 0.02% Sodium Azide as preservative and 50% Glycerol.
Storage instructions Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
Shipping Gel pack with blue ice.
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background Serine (phosphatidylserine, PS), also known as serine phospholipids, two acyl serine. Phosphate ester compounds in the glycerol phosphate esters, cell membrane group, is one of the important constituents of cell membranes in the brain, especially in the nervous system of the body and also various functions of the brain (especially on the brain's memory and emotional stability) plays important roles, such as it can affects the membrane fluidity and permeability, and can activate the metabolism and synthesis of a variety of enzymes.
Others The antibody detects endogenous Phosphoserine protein.

Image & description

Fig.1. Western blot analysis of 1) Hela, 2) Rat Brain Tissue, 3) Mouse Brain Tissue with Phosphoserine Mouse mAb diluted at 1:2000.

Fig.1. Western blot analysis of 1) Hela, 2) Rat Brain Tissue, 3) Mouse Brain Tissue with Phosphoserine Mouse mAb diluted at 1:2000.

Fig.2. Immunohistochemical analysis of paraffin-embedded Human Lung Caricnoma using Phosphoserine Mouse mAb diluted at 1:200.

Fig.2. Immunohistochemical analysis of paraffin-embedded Human Lung Caricnoma using Phosphoserine Mouse mAb diluted at 1:200.

Fig.3. Immunohistochemical analysis of paraffin-embedded Human Breast Caricnoma using Phosphoserine Mouse mAb diluted at 1:200.

Fig.3. Immunohistochemical analysis of paraffin-embedded Human Breast Caricnoma using Phosphoserine Mouse mAb diluted at 1:200.

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