Anti-Human MPO Monoclonal Antibody

The MPO gene encodes myeloperoxidase,a lysosomal hemoprotein located in the azurophilic granules of polymorphonuclear (PMN) leukocytes and monocytes. In response to stimulation,MPO is activated into a transient intermediate with potent antimicrobial oxidizing abilities. The mRNA is translated into a single protein of 90 kDa,which displays enzymatic activity and undergoes proteolytic maturation into a heavy chain of 59 kDa and a light chain of 13.5 kDa; these subunits then dimerize into the mature tetramer and the mature MPO is a heterotetramer composed of two identical heavy chains and two identical light chains. The 24-kDa material had a map identical to that of 13.5 kDa subunit and represents a dimer of the 13.5 kDa subunit . Defects in MPO are the cause of myeloperoxidase deficiency (MPOD). It has 3 isoforms produced by alternative splicing.
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Properties

Data Sheet Click for Datasheet
Catalog Number MA02040
Size 100μl
Host Type Mouse
Immunogen Fusion protein of MPO
Specificity
Isotype IgA
Reacitivity Human
Clone 9402
Uniprot P05164
Concentration None
Dilution WB 1:500-1:5000, IHC 1:20-1:200
Formulation
Application WB,IHC,ELISA
Other Names 84 kDa myeloperoxidase,89 kDa myeloperoxidase,EC 1.11.1.7,EC1.11.2.2,fj80f04,MPO,mpx,myeloid-specific peroxidase,Myeloperoxidase,Myeloperoxidase heavy chain,Myeloperoxidase light chain,PERM,wu:fj80f04
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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