Cell Signaling Technology

Product Pathways - Metabolism

NHERF2 (D3A5) Rabbit mAb #9568

Applications Reactivity Sensitivity MW (kDa) Isotype
W IP H Endogenous 46 Rabbit IgG

Applications Key:  W=Western Blotting  IP=Immunoprecipitation
Reactivity Key:  H=Human
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

NHERF2 (D3A5) Rabbit mAb recognizes endogenous levels of total NHERF2 protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human NHERF2 protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from MCF7 and T-47D cells using NHERF2 (D3A5) Rabbit mAb.

Background

Na+/H+ exchanger regulatory factor 2 (NHERF2) is one of four proteins in the NHERF protein family. It is closely related to NHERF1 and, like NHERF1, contains two PDZ domains and a C-terminal ezrin/radixin/moesin (ERM) binding domain (EBD). Along with the other members of this protein family, NHERF2 is abundantly present in the mammalian small intestine and colon where it plays a central role in trafficking, membrane retention, dimerization, and regulation of ion channels and membrane proteins (1). NHERF2 is a scaffolding protein that recruits membrane proteins to the apical membrane by tethering them to the apical cytoskeleton via its ERM domain (2). It has been shown that the NHERF proteins bind to the Na+/H+ exchanger 3 (NHE3) in the brush border of intestinal epithelial cells. NHE3 accounts for the majority of neutral NaCl absorbtion and NHERF proteins play an essential role in NHE3 regulation (3).

  1. Martinez, E. et al. (2010) Cell Microbiol 12, 1718-31.
  2. Enyedi, A. and Strehler, E.E. (2011) Commun Integr Biol 4, 340-3.
  3. Sarker, R. et al. (2011) Am J Physiol Cell Physiol 300, C771-82.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

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