Mouse Monoclonal Antibody to CD10

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Description

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.

Product Overview
Entrez GenelD
4311
Aliases
MME; NEP; SFE; CALLA
Clone#
1H8C10
Host / Isotype
Mouse / IgG2b
Immunogen
Purified recombinant fragment of human CD10 (AA: (651-750)) expressed in E. Coli.
Formulation
Purified antibody in PBS with 0.05% sodium azide
Storage
4℃; -20℃ for long term storage
Product Applications
WB (Western Blot)
1/500 - 1/2000
IHC_P(Immunohistochemistry)
1/200 - 1/1000
FCM (Flow Cytometry)
1/200 - 1/400
ELISA
1/10000
References
1,Pathol Res Pract. 2012 May 15;208(5):281-5.2,J Dermatol Sci. 2013 Feb;69(2):105-13.
Product Image
Elisa
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Western Blot
Figure 2:Western blot analysis using CD10 mAb against human CD10 (AA: (651-750)) recombinant protein. (Expected MW is 38.2 kDa)
Figure 2:Western blot analysis using CD10 mAb against human CD10 (AA: (651-750)) recombinant protein. (Expected MW is 38.2 kDa)
Western Blot
Figure 3:Western blot analysis using CD10 mAb against HEK293-6e (1) and CD10 (AA: (651-750))-hIgGFc transfected HEK293-6e (2) cell lysate.
Figure 3:Western blot analysis using CD10 mAb against HEK293-6e (1) and CD10 (AA: (651-750))-hIgGFc transfected HEK293-6e (2) cell lysate.
Western Blot
Figure 4:Western blot analysis using CD10 mouse mAb against Raji (1), Ramos (2), and LNcap (3) cell lysate.
Figure 4:Western blot analysis using CD10 mouse mAb against Raji (1), Ramos (2), and LNcap (3) cell lysate.
Flow cytometric analysis
Figure 5:Flow cytometric analysis of Hela cells using CD10 mouse mAb (green) and negative control (red).
Figure 5:Flow cytometric analysis of Hela cells using CD10 mouse mAb (green) and negative control (red).
Flow cytometric analysis
Figure 6:Flow cytometric analysis of THP-1 cells using CD10 mouse mAb (green) and negative control (red).
Figure 6:Flow cytometric analysis of THP-1 cells using CD10 mouse mAb (green) and negative control (red).
Immunohistochemical analysis
Figure 7:Immunohistochemical analysis of paraffin-embedded bladder cancer tissues using CD10 mouse mAb with DAB staining.
Figure 7:Immunohistochemical analysis of paraffin-embedded bladder cancer tissues using CD10 mouse mAb with DAB staining.
Immunohistochemical analysis
Figure 8:Immunohistochemical analysis of paraffin-embedded brain tissues using CD10 mouse mAb with DAB staining.
Figure 8:Immunohistochemical analysis of paraffin-embedded brain tissues using CD10 mouse mAb with DAB staining.
For Research Use Only. Not for use in diagnostic procedures.