POU4F3 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant POU4F3.
|Application ||WB, IF, E|
|Calculated MW||37052 Da|
|Other Names||POU domain, class 4, transcription factor 3, Brain-specific homeobox/POU domain protein 3C, Brain-3C, Brn-3C, POU4F3, BRN3C|
|Target/Specificity||POU4F3 (NP_002691, 100 a.a. ~ 190 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.|
|Format||Clear, colorless solution in phosphate buffered saline, pH 7.2 .|
|Storage||Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.|
|Precautions||POU4F3 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.|
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abgent to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
firstname.lastname@example.org, and receive a free "I Love Antibodies" mug.
Provided below are standard protocols that you may find useful for product applications.
This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.
A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss. Lee HK, et al. Biochem Biophys Res Commun, 2010 Jun 4. PMID 20434433.Molecular modelling insights into DFNA15 mediated enhancement of POU4F3 stability. Frenz CM, et al. Int J Comput Biol Drug Des, 2008. PMID 20054994.Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3. de Heer AM, et al. Ann Otol Rhinol Laryngol, 2009 Apr. PMID 19462854.Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3. van Drunen FJ, et al. Audiol Neurootol, 2009. PMID 19372648.Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3. Pauw RJ, et al. Arch Otolaryngol Head Neck Surg, 2008 Mar. PMID 18347256.
If you have used an Abgent product and would like to share how it has performed, please click on the "Submit Review" button and provide the requested information. Our staff will examine and post your review and contact you if needed.
If you have any additional inquiries please email technical services at email@example.com.