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Recombinant MME Antibody / CD10 / CALLA / Neprilysin

Recognizes a 100kDa glycoprotein, identified as CD10, also known as Membrane Metalloendopeptidase (MME), Common Acute Lymphocytic Leukemia Antigen (CALLA) and Neprilysin. It is a cell surface enzyme with neutral metalloendopeptidase activity, which inactivates a variety of biologically active peptides. CD10 is expressed on the cells of lymphoblastic, Burkitt s, and follicular germinal center lymphomas, and on cells from patients with chronic myelocytic leukemia (CML) . It is also expressed on the surface of normal early lymphoid progenitor cells, immature B cells within adult bone marrow and germinal center B cells within lymphoid tissue.CD10 is also present on breast myoepithelial cells, bile canaliculi, fibroblasts, with especially high expression on the brush border of kidney and gut epithelial cells.

Product Specifications

CAS Number

9000-83-3

Specifications

Immunohistochemistry (FFPE) : 1-2 µg/mL

UniProt

P08473

Host

Mouse

Reactivity

Human

Immunogen

Recombinant human CD10/Neprilysin protein fragment (amino acids 500-750) was used as the immunogen for the recombinant MME antibody.

Clonality

Recombinant Monoclonal

Isotype

IgG2b κ

Clone

RMME/9377

Type

Recombinant

Applications

IHC-P

Purity

Protein A/G affinity

Format

Purified

Buffer

1 mg/ml in 1X PBS; BSA free, sodium azide free

Reconstitution

Aliquot the recombinant MME antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Limitations

This recombinant MME antibody is available for research use only.

Storage Conditions

Aliquot the recombinant MME antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Formulation

1 mg/mL in 1X PBS; BSA free, sodium azide free

Applications Notes

Optimal dilution of the recombinant MME antibody should be determined by the researcher.

Location

Cytoplasm, Cell membrane

Image Legend

IHC staining of FFPE human prostate tissue with recombinant MME antibody (clone rMME/9377) . Inset: PBS used in place of primary Ab (secondary Ab negative control) . HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.
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