HOMER3 Products

Antibodies
HOMER3 Antibody
HOMER3 Antibody
Species: Hu
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
HOMER3 Antibody
HOMER3 Antibody
H00009454-B01P
Species: Hu
Applications: WB, ELISA
Host: Mouse Polyclonal
Lysates
HOMER3 Overexpression Lysate
HOMER3 Overexpression Lysate
NBP2-09758
Species: Hu
Applications: WB
HOMER3 Overexpression Lysate
HOMER3 Overexpression Lysate
NBL1-11657
Species: Hu
Applications: WB
Proteins
HOMER3 Recombinant Protein An ...
HOMER3 Recombinant Protein Antigen
NBP2-32607PEP
Species: Hu
Applications: AC
Recombinant Human HOMER3 Prot ...
Recombinant Human HOMER3 Protein
NBP1-98979
Species: Hu
Applications: PAGE

Description

This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. The encoded protein may be involved in cell growth.

Bioinformatics

Entrez Human
Rat
Uniprot Human
Human
Human
Rat
Product By Gene ID 9454
Alternate Names
  • Homer-3
  • Homer, neuronal immediate early gene, 3
  • homer protein homolog 3
  • VESL3
  • HOMER-3
  • homer homolog 3 (Drosophila)

Pathways for HOMER3

View related products by pathway and learn more about each of the pathways below.

Cell Activation
Membrane Depolarization
Mrna Transcription
Regulation Of T Cell Activation
T Cell Activation
Localization
Secretion

Research Areas for HOMER3

Find related products by research area and learn more about each of the different research areas below.

Neuroscience
Phospho-Specific

PTMs for HOMER3

Learn more about PTMs related to HOMER3.

Phosphorylation
Dephosphorylation

Bioinformatics Tool for HOMER3

Discover related pathways, diseases and genes to HOMER3. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
Vizit™, under license from BioVista Inc.

Related HOMER3 Blog Posts

Check out the latest blog posts on HOMER3.
RNA-binding protein Staufen1 conspires with Atxn2 in stress granules to cause neurodegeneration by dysregulating RNA metabolism
By Jamshed Arslan Pharm.D. Spinocerebellar ataxia type 2 (SCA2) is a movement disorder characterized by neurodegeneration. The cause of this autosomal dominant disease is a mutation in the RNA processing gene Atxn2,...    Read more.
Read more HOMER3 related blogs.