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For research use only.

Verified Samples Verified Samples in WB: RAW264.7, Mouse spleen, Mouse liver, Mouse lymph node, Rat spleen, Rat liver
Verified Samples in IHC: Mouse spleen, Rat spleen
Dilution WB 1:500-1:2000,  IHC 1:300-1:800
Isotype IgG
Host Rabbit
Reactivity Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen KLH conjugated Synthetic peptide corresponding to Mouse Lysozyme
Abbre Lysozyme
Synonyms 1,  1 4 beta N acetylmuramidase C,  4-beta-N-acetylmuramidase C,  EC 3.2.1.17,  LYSC,  LYZ,  LZM,  Lysosyme,  Lysozyme (renal amyloidosis),  Lysozyme C,  Lysozyme C precursor,  Renal amyloidosis
Swissprot
Calculated MW 17 kDa
Observed MW 17 kDa

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Secreted
Concentration 480 μg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 1% protein protectant and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cardiovascular,  Immunology,  Tags and Cell Markers
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background LYZ(Lysozyme C) is also named as LZM and belongs to the glycosyl hydrolase 22 family. It catalyzes the hydrolysis of the bacterial cell wall beta(1-4) glycosidic linkages between N-acetylmuramic acid and N-acetylglucosamine. In tissues and body fluids this protein is associated with the monocyte-macrophage system and enhance the activity of immunoagents. LYZ is capable of both hydrolysis and transglycosylation; it shows also a slight esterase activity. Defects in LYZ are a cause of amyloidosis type 8 (AMYL8). The full length protein has a signal peptide with 18 amino acid.
Other Clones

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Unconjugated

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