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POU4F3 Antibody

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Western Blot: POU4F3 Antibody [NBP1-52036] - Analysis of POU4F3 in Human Heart lysate (35ug protein in RIPA buffer) at 0.2ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.

Product Details

Summary
Reactivity Hu, Mu, Rt, CaSpecies Glossary
Applications WB, ELISA
Clonality
Polyclonal
Host
Goat
Conjugate
Unconjugated
Concentration
0.5 mg/ml

Order Details

POU4F3 Antibody Summary

Immunogen
Peptide with sequence C-EAAYREKNSKPE corresponding to internal region according to NP_002691.1.
Epitope
C-EAAYREKNSKPE
Specificity
This antibody is expected not to cross-react to the similar POU4F1 and POU4F2.
Predicted Species
Rat (100%), Canine (100%). Backed by our 100% Guarantee.
Isotype
IgG
Clonality
Polyclonal
Host
Goat
Gene
POU4F3
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Peptide ELISA Detection limit 1:8000
  • Western Blot 0.2 - 0.6 ug/ml
Application Notes
WB: Approx. 40 kDa band observed in human and mouse heart lysates (calculated MW of 37.1 kDa band according to human NP_002691.1).
Publications
Read Publication using NBP1-52036.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
Tris saline (20 mM Tris pH 7.3, 150 mM NaCl), 0.5% BSA
Preservative
0.02% Sodium Azide
Concentration
0.5 mg/ml
Purity
Immunogen affinity purified

Alternate Names for POU4F3 Antibody

  • brain-3C
  • Brain-specific homeobox/POU domain protein 3C
  • BRN3.1
  • Brn-3C
  • BRN3Cbrn-3C
  • DFNA15
  • MGC138412
  • POU class 4 homeobox 3
  • POU domain class 4, transcription factor 3
  • POU domain, class 4, transcription factor 3

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. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Publications for POU4F3 Antibody (NBP1-52036)(1)

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Product General Protocols

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Video Protocols

WB Video Protocol

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol POU4F3
Entrez
Uniprot