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Lysozyme Antibody

Catalog Number:

48872
other_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

Amount:

100μg
calculated_mw: 17 kDa
host_species: Rabbit

Price:

$319

Swiss-Prot No:

Swiss-Prot#:P61626

Form of Antibody:

1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.

Storage/Stability:

Immunogen:

recombinant protein

Purification:

ProA affinity purified

Specificity/Sensitivity:

Applications:

WB, ICC/IF, IHC, IP

Background:

The origins of the lysozyme proteins date back an estimated 400 to 600 million years. Generally, lysozyme genes are relatively small, roughly 10 kilobases in length, and composed of four exons and three introns. Originally a bacteriolytic defensive agent, the function of this family of proteins adapted to serve a digestive function in its present forms. Lysozymes in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents. Lysozyme C belongs to the glycosyl hydrolase 22 family, and newly identified relatives of Lysozyme C appear to possess anti-HIV activity, as well as preserved bacteriolytic function against Micrococcus lysodeikticus. Lysozyme C is capable of both hydrolysis and transglycosylation and also a slight esterase activity. It acts rapidly on both peptide-substituted and unsubstituted peptidoglycan, and slowly on chitin oligosaccharides. Lysozyme C defects are a cause of amyloidosis VIII, also called familial visceral or Ostertag-type amyloidosis.

References:

appl_detail:

WB: 1:1,000-1:2,000
IHC: 1:200-1:500
ICC: 1:50-1:200

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