LYZ polyclonal, anti-human, mouse
€388.00
In stock
SKU
BS7720
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.
Alternative Name:
1 4 beta N acetylmuramidase C, 1, 4-beta-N-acetylmuramidase C, EC 3.2.1.17, LYSC_HUMAN, Lysosyme, Lysozyme (renal amyloidosis), Lysozyme C, Lysozyme C precursor, LYZ, LZM, Renal amyloidosis,
Application Dilution: WB: 1:500~1:2000, IHC/IF: 1:50~1:200, IP: 1:20 - 1:50
Specificity: LYZ polyclonal antibody detects endogenous levels of LYZ protein.
Immunogen:
Recombinant full length Human LYZ.
MW: ~ 17 kDa
Swis Prot.: P61626
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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.
Alternative Name:
1 4 beta N acetylmuramidase C, 1, 4-beta-N-acetylmuramidase C, EC 3.2.1.17, LYSC_HUMAN, Lysosyme, Lysozyme (renal amyloidosis), Lysozyme C, Lysozyme C precursor, LYZ, LZM, Renal amyloidosis,
Application Dilution: WB: 1:500~1:2000, IHC/IF: 1:50~1:200, IP: 1:20 - 1:50
Specificity: LYZ polyclonal antibody detects endogenous levels of LYZ protein.
Immunogen:
Recombinant full length Human LYZ.
MW: ~ 17 kDa
Swis Prot.: P61626
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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