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Proteintech
DFNA5 Polyclonal Antibody
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Product Details
13075-1-AP
Applications
Tested Dilution
Publications
Product Specifications
Species Reactivity
Human,
Mouse
Published species
Human,
Mouse
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
DFNA5 Fusion Protein Ag3746 (111-460 aa encoded by BC019689)
Conjugate
Form
Liquid
Concentration
0.3 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice (domestic); Dry ice (international)
Product Specific Information
Immunogen sequence: SQSSFGTLR KQEVDLQQLI RDSAERTINL RNPVLQQVLE GRNEVLCVLT QKITTMQKCV ISEHMQVEEK CGGIVGIQTK TVQVSATEDG NVTKDSNVVL EIPAATTIAY GVIELYVKLD GQFEFCLLRG KQGGFENKKR IDSVYLDPLV FREFAFIDMP DAAHGISSQD GPLSVLKQAT LLLERNFHPF AELPEPQQTA LSDIFQAVLF DDELLMVLEP VCDDLVSGLS PTVAVLGELK PRQQQDLVAF LQLVGCSLQG GCPGPEDAGS KQLFMTAYFL VSALAEMPDS AAALLGTCCK LQIIPTLCHL LRALSDDGVS DLEDPTLTPL KDTERFGIVQ RLFASADISL (111-460 aa encoded by BC019689)
Target Information
DFNA5 (deafness, autosomal dominant 5), also known as ICERE-1, is a 496 amino acid protein that is expressed in cochlea tissue, as well as in placenta, brain, heart, liver, lung and pancreas as two alternatively spliced isoforms, designated short and long. Defects in the gene encoding DFNA5 are the cause of non-syndromic sensorineural deafness autosomal dominant type 5 (DFNA5), a form of sensorineural hearing loss that results from damage to one of various structures that receive sound information in the brain. The gene encoding DFNA5 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Bioinformatics
Protein Aliases: deafness, autosomal dominant 5; deafness, autosomal dominant 5 homolog; Gasdermin-E; ICERE-1; Inversely correlated with estrogen receptor expression 1; Non-syndromic hearing impairment protein 5; Non-syndromic hearing impairment protein 5 homolog; nonsyndromic hearing impairment protein
Gene Aliases: 2310037D07Rik; 4932441K13Rik; DFNA5; Dfna5h; EG14210; Fin15; GSDME; ICERE-1; ICERE1
UniProt ID: (Human) O60443, (Mouse) Q9Z2D3
Entrez Gene ID: (Human) 1687, (Mouse) 54722
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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