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Anti-Lysozyme antibody (ab34799)

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Overview

Product name

Anti-Lysozyme antibody
See all Lysozyme products (16) ...

Description

Rabbit polyclonal to Lysozyme

Specificity

ab34799 recognises purified and partially purified Lysozyme.

Tested applications

Dot Blot, WB, ELISA, IPmore details

Cross reactivity

Reacts with

Chicken

Immunogen

Full length native protein (purified): Lysozyme from Hen Egg White.

Properties

Form

Liquid

Storage instructions

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.

Storage buffer

Preservative: 0.01% Sodium Azide
Constituents: 0.14M Sodium chloride, 0.01M Sodium phosphate. pH 7.4

Concentration

Concentration information loading...

Purification notes

Purified from monospecific antiserum by a delipidation and defibrination.

Clonality

Polyclonal

Isotype

IgG

Applications

Show applications key

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.

Application notes

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.

Target

Function

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.

Involvement in disease

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.

Sequence similarities

Belongs to the glycosyl hydrolase 22 family.

Cellular localization

Secreted.

Target information above from: UniProt accessionP61626 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).

Information by UniProt

Alternative names

  • 1 4 beta n acetylmuramidase c antibody
  • 1 antibody
  • 4-beta-N-acetylmuramidase C antibody
  • EC 3.2.1.17 antibody
  • LYSC_HUMAN antibody
  • Lysosyme antibody
  • Lysozyme (renal amyloidosis) antibody
  • Lysozyme C antibody
  • Lysozyme C precursor antibody
  • Lyz antibody
  • LZM antibody
  • Renal amyloidosis antibody
see all

Database links

References for Anti-Lysozyme antibody (ab34799)

This product has been referenced in:

  • Akama Ket al. Protein disulfide isomerase-P5, down-regulated in the final stage of boar epididymal sperm maturation, catalyzes disulfide formation to inhibit protein function in oxidative refolding of reduced denatured lysozyme. Biochim Biophys Acta 1804:1272-84 (2010).Read more (PubMed: 20152940) »
  • Setälä NLet al. Interaction of phospholipid transfer protein with human tear fluid mucins. J Lipid Res 51:3126-34 (2010). WB; Human.Read more (PubMed: 20724654) »

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

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"