KRCC1 抗体 (Cy3)
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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, 大鼠
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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 conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human KRCC1
- 亚型
- IgG
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anti-Lysine-Rich Coiled-Coil 1 (KRCC1) antibody
KRCC1 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (AA 1-259) antibodyKRCC1 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (AA 35-84) antibodyKRCC1 适用: 人, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (N-Term) antibodyKRCC1 适用: 人, 马 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 1:50-200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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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
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Synonyms: CHBP2, cryptogenic hepatitis binding protein, Cryptogenic hepatitis-binding protein 2, KRCC1, KRCC1_HUMAN, lysine rich coiled coil 1, Lysine-rich coiled-coil protein 1.
Background: KRCC1 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, Alstr 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.
- 基因ID
- 51315
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