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Mouse anti-Human sapiens (Human) MPO Monoclonal Antibody

Mouse anti-Human sapiens (Human) MPO Monoclonal Antibody — (Microbial infection) The peroxidase activity is inhibited by S.

SKU: BCREC-000243MA Category:
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Product Specifications

Uniprot No.P05164
Target NamesMPO
Species Reactivitymouse
ImmunogenHuman Myeloperoxidase
Immunogen SpeciesHomo sapiens (Human)
ConjugateNon-conjugated
IsotypeIgG2a
ClonalityMonoclonal
ApplicationsELISA
BufferPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
StorageUpon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Function

(Microbial infection) The peroxidase activity is inhibited by S.aureus peroxidase inhibitor SPIN that blocks substrate access to the catalytic heme.

Biological Context

Subcellular Location: Lysosome; Cytolytic granule; Cytoplasmic vesicle, phagosome; Secreted; Nucleus; Chromosome
Tissue Specificity: Specifically expressed in neutrophils and monocytes
Disease Association: Myeloperoxidase deficiency (MPOD) : A disorder characterized by decreased myeloperoxidase activity in neutrophils and monocytes that results in disseminated candidiasis. [The disease is caused by variants affecting the gene represented in this entry]

Product Specifications

Mouse anti-Human sapiens (Human) MPO Monoclonal Antibody is a recombinant protein. Suitable for ELISA and Western Blot applications.

Applications: ELISA

Biological Activity: Not implied unless activity data are explicitly listed on this product page, the datasheet, or the CoA.

Storage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Shipping & Lead Time: Availability, shipping conditions, and estimated lead time are confirmed in the formal quotation or order confirmation based on the product format, destination, and order requirements.

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Protein Biology

Function

(Microbial infection) The peroxidase activity is inhibited by S.aureus peroxidase inhibitor SPIN that blocks substrate access to the catalytic heme

Subcellular Location

Lysosome; Cytolytic granule; Cytoplasmic vesicle, phagosome; Secreted; Nucleus; Chromosome

Disease Association

Myeloperoxidase deficiency (MPOD) : A disorder characterized by decreased myeloperoxidase activity in neutrophils and monocytes that results in disseminated candidiasis. [The disease is caused by variants affecting the gene represented in this entry]

Tissue Specificity

Specifically expressed in neutrophils and monocytes

Subunit

Mature myeloperoxidase is a homodimer; disulfide-linked (PubMed:2820530, PubMed:31719144). Each monomer is composed of myeloperoxidase heavy chain and myeloperoxidase light chain (PubMed:2820530, PubMed:31719144)

Gene: MPO  |  Organism: Homo sapiens
Key Publications

Explore closely related product collections, technology platforms, and custom production resources.

Frequently Asked Questions

How do I order or inquire about this product?

Submit the Online Inquiry form with your required quantity and specifications, or email sales@biocrestsci.com. Available sizes, pricing, stock status, documentation, and estimated lead time are confirmed in the formal quotation.

What is the shipping and delivery time?

Availability, dispatch timing, shipping conditions, and delivery estimates depend on the product format, destination, and order requirements. These details are confirmed in the formal quotation or order confirmation.

How should this product be stored?

Follow the storage and handling instructions in the product-specific datasheet and Certificate of Analysis (CoA). Requirements may vary by product form and formulation; contact BioCrest Sci if product-specific guidance is needed.

What quality controls are performed on your products?

Quality-control data such as identity, purity, endotoxin level, or biological activity are provided only when specified on this product page, the datasheet, or Certificate of Analysis (CoA). Biological activity is not implied unless explicitly stated.

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