MME Antibody

ProSci
Product Code: PSI-19-781
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-19-781-50uL50uL£433.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Shipping:
Blue Ice or RT
Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Images

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Western blot analysis of extracts of various cell lines, using MME antibody (19-781) at 1:1000 dilution.<br/>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br/>Lysates/proteins: 25ug per lane.<br/>Blocking buffer: 3% nonfat dry milk in TBST.<br/>Detection: ECL Basic Kit.<br/>Exposure time: 90s.
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Immunohistochemistry of paraffin-embedded rat testis using MME antibody (19-781) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded human placenta using MME antibody (19-781) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded mouse kidney using MME antibody (19-781) at dilution of 1:100 (40x lens).
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Immunofluorescence analysis of human placenta using MME antibody (19-781) at dilution of 1:100. Blue: DAPI for nuclear staining.

Western blot analysis of extracts of various cell lines, using MME antibody (19-781) at 1:1000 dilution.<br/>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br/>Lysates/proteins: 25ug per lane.<br/>Blocking buffer: 3% nonfat dry milk in TBST.<br/>Detection: ECL Basic Kit.<br/>Exposure time: 90s.
Immunohistochemistry of paraffin-embedded rat testis using MME antibody (19-781) at dilution of 1:100 (40x lens).
Immunohistochemistry of paraffin-embedded human placenta using MME antibody (19-781) at dilution of 1:100 (40x lens).
Immunohistochemistry of paraffin-embedded mouse kidney using MME antibody (19-781) at dilution of 1:100 (40x lens).
Immunofluorescence analysis of human placenta using MME antibody (19-781) at dilution of 1:100. Blue: DAPI for nuclear staining.

Further Information

Additional Names:
Neprilysin, Atriopeptidase, Common acute lymphocytic leukemia antigen, CALLA, Enkephalinase, Neutral endopeptidase 2411, NEP, Neutral endopeptidase, Skin fibroblast elastase, SFE, CD10, MME, EPN
Application Note:
WB: 1:500 - 1:2000

IHC: 1:50 - 1:200

IF: 1:50 - 1:200
Background:
This gene encodes a common acute lymphocytic leukemia antigen that is an important cell surface marker in the diagnosis of human acute lymphocytic leukemia (ALL). This protein is present on leukemic cells of pre-B phenotype, which represent 85% of cases of ALL. This protein is not restricted to leukemic cells, however, and is found on a variety of normal tissues. It is a glycoprotein that is particularly abundant in kidney, where it is present on the brush border of proximal tubules and on glomerular epithelium. The protein is a neutral endopeptidase that cleaves peptides at the amino side of hydrophobic residues and inactivates several peptide hormones including glucagon, enkephalins, substance P, neurotensin, oxytocin, and bradykinin. This gene, which encodes a 100-kD type II transmembrane glycoprotein, exists in a single copy of greater than 45 kb. The 5' untranslated region of this gene is alternatively spliced, resulting in four separate mRNA transcripts. The coding region is not affected by alternative splicing.
Buffer:
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentration:
batch dependent
Conjugate:
Unconjugated
DISCLAIMER:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 52-352 of human MME (NP_009220.2).
NCBI Gene ID #:
4311
NCBI Official Name:
membrane metallo-endopeptidase
NCBI Official Symbol:
MME
NCBI Organism:
Homo sapiens
Physical State:
Liquid
PREDICTED MOLECULAR WEIGHT:
Observed: 108kDa
Purification:
Affinity purification
Research Area:
Cancer, Immunology, Neuroscience, Stem Cell
Swissprot #:
P08473
User NOte:
Optimal dilutions for each application to be determined by the researcher.