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Read our guarantee »Products:Immunology >> Innate Immunity >> Macrophage / Inflamm.
Anti-Lysozyme antibody - Lysosome Marker
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Rabbit polyclonal to Lysozyme - Lysosome Marker
Assay by immunoelectrophoresis resulted in a single precipitin arc against purified and partially purified Lysozyme from hen egg white.
WB, IP, ELISAmore details
Reacts with
Chicken
Lysozyme from Hen Egg White
Assayed against 1.0 ug of Lysozyme from hen egg white in a standard sandwich ELISA using Peroxidase conjugated Affinity Purified anti-Rabbit IgG [H&L] (Goat) and (ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. 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...
IgG fraction
IgG fraction purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rabbit Serum as well as purified and partially purified Lysozyme.
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 ab391 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/4000 - 1/10000.
IP: 1/4000 - 1/10000.
ELISA: Use at an assay dependent dilution.
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
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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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