KRCC1 抗体
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- 抗原 See all KRCC1 products
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
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适用
- 人, 小鼠
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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 KRCC1 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 KRCC1
- 亚型
- IgG
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- 应用备注
- WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1.68 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
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
- 别名
- KRCC1 (KRCC1 产品)
- 别名
- DKFZp468N1119 antibody, CHBP2 antibody, AA792894 antibody, RGD1306495 antibody, lysine rich coiled-coil 1 antibody, lysine-rich coiled-coil 1 antibody, KRCC1 antibody, Krcc1 antibody
- 背景
- KRCC1 (lysine-rich coiled-coil 1), also known as CHBP2 (cryptogenic hepatitis-binding protein 2), is a 259 amino acid protein that is encoded by a gene located on human chromosome 2p11.2. Consisting of 237 million bases, chromosome 2 is the second largest human chromosome and encodes over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome, is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- 分子量
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Observed_MW: Refer to figures
Calculated_MW: 31 kDa
- UniProt
- Q9NPI7
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