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Read our guarantee »Products:Immunology >> Innate Immunity >> Macrophage / Inflamm.
Anti-Lysozyme antibody
See all Lysozyme products (16) ...
Rabbit polyclonal to Lysozyme
ab34799 recognises purified and partially purified Lysozyme.
Dot Blot, WB, ELISA, IPmore details
Reacts with
Chicken
Full length native protein (purified): Lysozyme from Hen Egg White.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.01% Sodium Azide
Constituents: 0.14M Sodium chloride, 0.01M Sodium phosphate. pH 7.4
Concentration information loading...
Purified from monospecific antiserum by a delipidation and defibrination.
Polyclonal
IgG
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Lysosome
Cardiovascular >> Blood >> Other
Immunology >> Adaptive Immunity >> T Cells >> Cytotoxic Cells
Immunology >> Innate Immunity >> Macrophage / Inflamm.
Our Abpromise guarantee covers the use of ab34799 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Dot: Use at an assay dependent dilution.
ELISA: 1/1,000 - 1/2,000.
IP: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution. Predicted molecular weight: 17 kDa.
This product has been assayed against 1.0 µg of Lysozyme in a standard sandwich ELISA using Peroxidase conjugated Afinity Purified anti-Rabbit IgG and ABTS (2,2'-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid))as a substrate for 30 minutes at room temperature.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents.
Defects in LYZ are a cause of amyloidosis type 8 (AMYL8) [MIM:105200]; also known as systemic non-neuropathic amyloidosis or Ostertag-type amyloidosis. AMYL8 is a hereditary generalized amyloidosis due to deposition of apolipoprotein A1, fibrinogen and lysozyme amyloids. Viscera are particularly affected. There is no involvement of the nervous system. Clinical features include renal amyloidosis resulting in nephrotic syndrome, arterial hypertension, hepatosplenomegaly, cholestasis, petechial skin rash.
Belongs to the glycosyl hydrolase 22 family.
Secreted.
Target information above from: UniProt accessionP61626
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
This product has been referenced in:
See all 2 publications for this product
Publishing research using ab34799? Please let us know so that we can cite the reference in this datasheet
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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