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Anti-MAPRE2 / EB2 Antibody (clone 3C4) LS-C172958

Ordering

Wt. Vol. Conc. Price
- 100 µl 0.62 mg/ml $325
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular MAPRE2 / EB2 Antibodies

Anti-MAPRE2 / EB2 Antibody (clone 1F3) IHC-plus™ LS-B9959
Mouse Monoclonal [clone 1F3] (IgG2a) to Human MAPRE2 / EB2
Human
IHC - Paraffin, Immunofluorescence, Western blot, Flow Cytometry
Unconjugated
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Mouse Monoclonal [clone 3C4] (IgG1) to Human MAPRE2 / EB2
Human
Immunofluorescence, Western blot, Flow Cytometry
Unconjugated

Details

Human MAPRE2 / EB2
Mouse
Human (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [3C4]
Unconjugated
Protein A/G purified
Unmodified

Applications

  • Immunofluorescence (1:100)
  • Western blot (1:2000)
  • Flow Cytometry (1:100)

Specificity and Use

MAPRE2 / EB2 antibody was raised against full length human recombinant protein of human MAPRE2 (NP_055083) produced in HEK293T cell.
Human MAPRE2 / EB2

Packaging

PBS, pH 7.3, 1% BSA, 50% glycerol, 0.02% sodium azide
Store at -20°C. Minimize freezing and thawing.
For research use only.

About MAPRE2 / EB2

Q15555 NM_014268 NP_055083.1

MAPRE2 Antibody, APC-binding protein EB2 Antibody, APC-binding protein EB1 Antibody, EB1 Antibody, EB2 Antibody, End-binding protein 2 Antibody

MAPRE2 / EB2 shares significant homology to the adenomatous polyposis coli (APC) protein-binding EB1 gene family. This protein is a microtubule-associated protein that is necessary for spindle symmetry during mitosis. It is thought to play a role in the tumorigenesis of colorectal cancers and the proliferative control of normal cells. Alternative splicing of this gene results in multiple transcript variants.

Immunofluorescence

Immunofluorescence
Anti-MAPRE2 mouse monoclonal antibody immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY MAPRE2.

Western blot

Western blot
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MAPRE2 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-MAPRE2.

Flow Cytometry

Flow Cytometry
Flow cytometry of Jurkat cells, using anti-MAPRE2 antibody (Red), compared to a nonspecific negative control antibody (Blue).
 

Requested From: United States
Date Requested: 12/9/2016

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