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- References [5]
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- Product number
- ABIN395693 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Methylcrotonoyl-CoA Carboxylase 1 (Alpha) (MCCC1) (AA 526-626) 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 526-626
- Isotype
- IgG
- Antibody clone number
- 2G8
- 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 Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Cryptic exon activation by disruption of exon splice enhancer: novel mechanism causing 3-methylcrotonyl-CoA carboxylase deficiency.
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
Toward a confocal subcellular atlas of the human proteome.
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency.
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
Cryptic exon activation by disruption of exon splice enhancer: novel mechanism causing 3-methylcrotonyl-CoA carboxylase deficiency.
Stucki M, Suormala T, Fowler B, Valle D, Baumgartner MR
The Journal of biological chemistry 2009 Oct 16;284(42):28953-7
The Journal of biological chemistry 2009 Oct 16;284(42):28953-7
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
Eminoglu FT, Ozcelik AA, Okur I, Tumer L, Biberoglu G, Demir E, Hasanoglu A, Baumgartner MR
Journal of child neurology 2009 Apr;24(4):478-81
Journal of child neurology 2009 Apr;24(4):478-81
Toward a confocal subcellular atlas of the human proteome.
Barbe L, Lundberg E, Oksvold P, Stenius A, Lewin E, Björling E, Asplund A, Pontén F, Brismar H, Uhlén M, Andersson-Svahn H
Molecular & cellular proteomics : MCP 2008 Mar;7(3):499-508
Molecular & cellular proteomics : MCP 2008 Mar;7(3):499-508
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency.
Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T
Journal of human genetics 2007;52(12):1040-3
Journal of human genetics 2007;52(12):1040-3
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Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- ELISA
