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- Product number
- ABIN953167 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5) (AA 193-222), (C-Term) antibody
- Antibody type
- Polyclonal
- Description
- Protein A column, followed by peptide affinity purification
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- C-Term, AA 193-222
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Unique transgenic animal model for hereditary hearing loss.
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Cosetti M, Culang D, Kotla S, O'Brien P, Eberl DF, Hannan F
The Annals of otology, rhinology, and laryngology 2008 Nov;117(11):827-33
The Annals of otology, rhinology, and laryngology 2008 Nov;117(11):827-33
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
Shabbir MI, Ahmed ZM, Khan SY, Riazuddin S, Waryah AM, Khan SN, Camps RD, Ghosh M, Kabra M, Belyantseva IA, Friedman TB, Riazuddin S
Journal of medical genetics 2006 Aug;43(8):634-40
Journal of medical genetics 2006 Aug;43(8):634-40
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Longo-Guess CM, Gagnon LH, Cook SA, Wu J, Zheng QY, Johnson KR
Proceedings of the National Academy of Sciences of the United States of America 2005 May 31;102(22):7894-9
Proceedings of the National Academy of Sciences of the United States of America 2005 May 31;102(22):7894-9
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