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- Product number
- ABIN395383 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Ankyrin Repeat Domain 15 (ANKRD15) (AA 701-800) 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
- Host
- Mouse
- Epitope
- AA 701-800
- Isotype
- IgG
- Antibody clone number
- 2B8
- 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 KANK1, a candidate tumor suppressor gene, is fused to PDGFRB in an imatinib-responsive myeloid neoplasm with severe thrombocythemia.
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane.
Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
Risk alleles for multiple sclerosis in multiplex families.
Medves S, Duhoux FP, Ferrant A, Toffalini F, Ameye G, Libouton JM, Poirel HA, Demoulin JB
Leukemia 2010 May;24(5):1052-5
Leukemia 2010 May;24(5):1052-5
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR
Molecular medicine (Cambridge, Mass.) 2010 Jul-Aug;16(7-8):247-53
Molecular medicine (Cambridge, Mass.) 2010 Jul-Aug;16(7-8):247-53
A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane.
Kakinuma N, Kiyama R
Biochemical and biophysical research communications 2009 Sep 4;386(4):639-44
Biochemical and biophysical research communications 2009 Sep 4;386(4):639-44
Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
Hoppenbrouwers IA, Aulchenko YS, Janssens AC, Ramagopalan SV, Broer L, Kayser M, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ
Journal of human genetics 2009 Nov;54(11):676-80
Journal of human genetics 2009 Nov;54(11):676-80
Risk alleles for multiple sclerosis in multiplex families.
D'Netto MJ, Ward H, Morrison KM, Ramagopalan SV, Dyment DA, DeLuca GC, Handunnetthi L, Sadovnick AD, Ebers GC
Neurology 2009 Jun 9;72(23):1984-8
Neurology 2009 Jun 9;72(23):1984-8
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Supportive validation
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- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- ELISA
