DFNA5 purified MaxPab mouse polyclonal antibody (B02P)
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More Files
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Specifications
Product Description
Mouse polyclonal antibody raised against a full-length human DFNA5 protein.
Immunogen
DFNA5 (NP_004394.1, 1 a.a. ~ 496 a.a) full-length human protein.
Sequence
MFAKATRNFLREVDADGDLIAVSNLNDSDKLQLLSLVTKKKRFWCWQRPKYQFLSLTLGDVLIEDQFPSPVVVESDFVKYEGKFANHVSGTLETALGKVKLNLGGSSRVESQSSFGTLRKQEVDLQQLIRDSAERTINLRNPVLQQVLEGRNEVLCVLTQKITTMQKCVISEHMQVEEKCGGIVGIQTKTVQVSATEDGNVTKDSNVVLEIPAATTIAYGVIELYVKLDGQFEFCLLRGKQGGFENKKRIDSVYLDPLVFREFAFIDMPDAAHGISSQDGPLSVLKQATLLLERNFHPFAELPEPQQTALSDIFQAVLFDDELLMVLEPVCDDLVSGLSPTVAVLGELKPRQQQDLVAFLQLVGCSLQGGCPGPEDAGSKQLFMTAYFLVSALAEMPDSAAALLGTCCKLQIIPTLCHLLRALSDDGVSDLEDPTLTPLKDTERFGIVQRLFASADISLERLKSSVKAVILKDSKVFPLLLCITLNGLCALGREHS
Host
Mouse
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of DFNA5 expression in transfected 293T cell line (H00001687-T02) by DFNA5 MaxPab polyclonal antibody.
Lane 1: DFNA5 transfected lysate(54.56 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — DFNA5
Entrez GeneID
1687GeneBank Accession#
NM_004403Protein Accession#
NP_004394.1Gene 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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Interactomes
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Diseases
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