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Lysozyme Recombinant antibody, PBS Only

Lysozyme Uni-rAbTM Recombinant Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

CloneNo.

241054E1

Cat no : 84140-1-PBS

Synonyms

LYZ, LZM, Lysozyme C, EC:3.2.1.17, 241054E1

Validation Data Gallery

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  • Western Blot (WB) analysis of human saliva using Lysozyme Recombinant antibody (84140-1-RR)

    WB analysis of human saliva using 84140-1-RR (same clone as 84140-1-PBS)

    human saliva were subjected to SDS PAGE followed by western blot with 84140-1-RR (Lysozyme antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 84140-1-PBS in a different storage buffer formulation.

  • Affinity and Kinetic Characterization of 84140-1-RR

    Affinity and Kinetic Characterization of 84140-1-RR

    Biolayer interferometry (BLl) kinetic assays of 84140-1-RR against Human Lysozyme were performed. The affinity constant is 133 nM.

Product Information

The immunogen of 84140-1-PBS is Lysozyme Fusion Protein expressed in E. coli.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen Lysozyme fusion protein Ag6917
Full Name lysozyme (renal amyloidosis)
Calculated Molecular Weight 17 kDa
Observed Molecular Weight10 kDa
GenBank Accession NumberBC004147
Gene Symbol Lysozyme
Gene ID (NCBI) 4069
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

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.