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- 抗原 See all C15orf40 products
- C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))
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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 C15orf40 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Fusion protein of human C15orf40
- 亚型
- IgG
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anti-Chromosome 15 Open Reading Frame 40 (C15orf40) antibody
C15orf40 适用: 人 WB, IHC, FACS 宿主: 小鼠 Monoclonal 2B7 unconjugated
anti-Chromosome 15 Open Reading Frame 40 (C15orf40) (C-Term) antibodyC15orf40 适用: 人, 小鼠, Cow, 犬, 豚鼠, 马, 大鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 15 Open Reading Frame 40 (C15orf40) (AA 72-100), (C-Term) antibodyC15orf40 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB31462 unconjugated
anti-Chromosome 15 Open Reading Frame 40 (C15orf40) (AA 79-108), (C-Term) antibodyC15orf40 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.5 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
- C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))
- 别名
- C15orf40 (C15orf40 产品)
- 别名
- MGC89060 antibody, AI851475 antibody, C15orf40 antibody, c15orf40 antibody, chromosome 15 open reading frame 40 antibody, RIKEN cDNA 3110040N11 gene antibody, similar to RIKEN cDNA 3110040N11 antibody, chromosome 21 open reading frame, human C15orf40 antibody, chromosome 15 open reading frame 40 L homeolog antibody, C15orf40 antibody, c15orf40 antibody, 3110040N11Rik antibody, RGD1305713 antibody, C21H15orf40 antibody, c15orf40.L antibody
- 背景
- Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.
- 分子量
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Observed_MW: Refer to figures
Calculated_MW: 16 kDa
- UniProt
- Q8WUR7
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