IQCA1 抗体
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- 抗原 See all IQCA1 抗体
- IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
- 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 IQCA1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 IQCA1
- 亚型
- IgG
- Top Product
- Discover our top product IQCA1 Primary Antibody
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anti-IQ Motif Containing with AAA Domain 1 (IQCA1) (AA 794-822), (C-Term) antibody
IQCA1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB31637 unconjugated
anti-IQ Motif Containing with AAA Domain 1 (IQCA1) (AA 791-822), (C-Term) antibodyIQCA1 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
- 别名
- IQCA1 (IQCA1 产品)
- 别名
- 4930465P12Rik antibody, 4930585L22Rik antibody, BB288505 antibody, Iqca1 antibody, IQCA antibody, RGD1305311 antibody, IQ motif containing with AAA domain antibody, IQ motif containing with AAA domain 1 antibody, Iqca antibody, IQCA1 antibody, Iqca1 antibody
- 背景
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Synonyms: IQ and AAA domain-containing protein 1, IQ mot containing with AAA domain 1, IQCA, Iqca1, IQCA1_HUMAN, RGD1305311, FLJ22527, 4930465P12Rik, FLJ33588.
Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. 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.
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