DFNA5 polyclonal antibody
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More Files
- More Functions
Western Blot (Cell lysate)
Western Blot analysis of HepG2 cell lysate with DFNA5 polyclonal antibody (Cat # PAB30029) at 1.25 ug/mL working concentration.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with DFNA5 polyclonal antibody (Cat # PAB30029) at 4-8 ug/mL working concentration.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of human DFNA5.
Immunogen
A synthetic peptide corresponding to C-terminus of human DFNA5.
Sequence
AALLGTCCKLQIIPTLCHLLRALSDDGVSDLEDPTLTPLKDTERFGIVQR
Host
Rabbit
Theoretical MW (kDa)
47
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (4-8 ug/mL)
Western Blot (1.25 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (2% sucrose, 0.09% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western Blot analysis of HepG2 cell lysate with DFNA5 polyclonal antibody (Cat # PAB30029) at 1.25 ug/mL working concentration.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with DFNA5 polyclonal antibody (Cat # PAB30029) at 4-8 ug/mL working concentration. -
Gene Info — DFNA5
Entrez GeneID
1687GeneBank Accession#
NM_001127453Protein Accession#
AAI25067;A4FVA8Gene Name
DFNA5
Gene Alias
ICERE-1
Gene Description
deafness, autosomal dominant 5
Gene Ontology
HyperlinkGene Summary
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq
Other Designations
deafness, autosomal dominant 5 protein|inversely correlated with estrogen receptor expression 1|nonsyndromic hearing impairment protein
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Interactome
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Disease
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