POU4F3 antibody (clone 5B8), anti-human
€435.00
In stock
SKU
AC-AT3386a
Catalog Number: AC-AT3386a
Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, IF, E
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Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, IF, E
Request Information AC-AT3386a">Request Information
Background:
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.
Other Names:
POU domain, class 4, transcription factor 3, Brain-specific homeobox/POU domain protein 3C, Brain-3C, Brn-3C, POU4F3, BRN3C
Antigen Type:
Recombinant Protein
Gene Name: POU4F3
Gene ID: 5459
NCBI Accession: NP_002691.1
Primary Accession: Q15319
Other Accession: NM_002700
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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.
Other Names:
POU domain, class 4, transcription factor 3, Brain-specific homeobox/POU domain protein 3C, Brain-3C, Brn-3C, POU4F3, BRN3C
Antigen Type:
Recombinant Protein
Gene Name: POU4F3
Gene ID: 5459
NCBI Accession: NP_002691.1
Primary Accession: Q15319
Other Accession: NM_002700
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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