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- 抗原 See all C12orf40 products
- C12orf40 (Chromosome 12 Open Reading Frame 40 (C12orf40))
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This C12orf40 antibody is un-conjugated
- 应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Fusion protein of human C12orf40
- 亚型
- IgG
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anti-Chromosome 12 Open Reading Frame 40 (C12orf40) (AA 1-422) antibody
C12orf40 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 40 (C12orf40) (AA 146-195) antibodyC12orf40 适用: 人, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 40 (C12orf40) (N-Term) antibodyC12orf40 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 40 (C12orf40) (N-Term) antibodyC12orf40 适用: 人, Pig, 马 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:40-1:200, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- C12orf40 (Chromosome 12 Open Reading Frame 40 (C12orf40))
- 别名
- C12orf40 (C12orf40 产品)
- 别名
- chromosome 12 open reading frame 40 antibody, C12orf40 antibody
- 背景
- Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf40 gene product has been provisionally designated C12orf40 pending further characterization.
- UniProt
- Q86WS4
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