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- Product number
- ABIN955258 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Transmembrane Inner Ear (TMIE) (AA 78-108), (Middle Region) antibody
- Antibody type
- Polyclonal
- Description
- Protein A column followed by peptide affinity purification
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 78-108, Middle Region
- Vial size
- 0.4 mL
- Storage
- Store at 2 - 8°C for up to six months or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.
Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
Santos RL, El-Shanti H, Sikandar S, Lee K, Bhatti A, Yan K, Chahrour MH, McArthur N, Pham TL, Mahasneh AA, Ahmad W, Leal SM
Journal of molecular medicine (Berlin, Germany) 2006 Mar;84(3):226-31
Journal of molecular medicine (Berlin, Germany) 2006 Mar;84(3):226-31
Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
Cho KI, Lee JW, Kim KS, Lee EJ, Suh JG, Lee HJ, Kim HT, Hong SH, Chung WH, Chang KT, Hyun BH, Oh YS, Ryoo ZY
Comparative medicine 2003 Dec;53(6):642-8
Comparative medicine 2003 Dec;53(6):642-8
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER
American journal of human genetics 2002 Sep;71(3):632-6
American journal of human genetics 2002 Sep;71(3):632-6
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC
Human molecular genetics 2002 Aug 1;11(16):1887-98
Human molecular genetics 2002 Aug 1;11(16):1887-98
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