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- Product number
- ABIN393308 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 4 (KCNQ4) (AA 596-696) antibody
- Antibody type
- Monoclonal
- Description
- This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Reactivity
- Human, Mouse
- Host
- Mouse
- Epitope
- AA 596-696
- Isotype
- IgG
- Antibody clone number
- 2H6
- Vial size
- 100 μg
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Submitted references Replication of previous genome-wide association studies of bone mineral density in premenopausal American women.
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss.
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.
DFNA2 Nonsyndromic Hearing Loss
Ichikawa S, Koller DL, Padgett LR, Lai D, Hui SL, Peacock M, Foroud T, Econs MJ
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2010 Aug;25(8):1821-9
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2010 Aug;25(8):1821-9
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss.
Pawelczyk M, Van Laer L, Fransen E, Rajkowska E, Konings A, Carlsson PI, Borg E, Van Camp G, Sliwinska-Kowalska M
Annals of human genetics 2009 Jul;73(Pt 4):411-21
Annals of human genetics 2009 Jul;73(Pt 4):411-21
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
Nie L
Current opinion in otolaryngology & head and neck surgery 2008 Oct;16(5):441-4
Current opinion in otolaryngology & head and neck surgery 2008 Oct;16(5):441-4
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.
Hildebrand MS, Tack D, McMordie SJ, DeLuca A, Hur IA, Nishimura C, Huygen P, Casavant TL, Smith RJ
Genetics in medicine : official journal of the American College of Medical Genetics 2008 Nov;10(11):797-804
Genetics in medicine : official journal of the American College of Medical Genetics 2008 Nov;10(11):797-804
DFNA2 Nonsyndromic Hearing Loss
Smith RJH, Hildebrand M, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A
1993;
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Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC
