CCDC93 抗体 (AA 531-631) (AbBy Fluor® 647)
Quick Overview for CCDC93 抗体 (AA 531-631) (AbBy Fluor® 647) (ABIN888356)
抗原
See all CCDC93 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 531-631
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交叉反应
- 大鼠
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预测反应
- Human,Mouse,Dog,Cow,Sheep,Pig
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human CCDC93
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 93 (CCDC93) (AA 293-631) antibody
CCDC93 适用: 人, 犬, 猴 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 6E11 unconjugated
anti-Coiled-Coil Domain Containing 93 (CCDC93) (C-Term) antibodyCCDC93 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 93 (CCDC93) (AA 1-631) antibodyCCDC93 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 93 (CCDC93) (AA 293-631) antibodyCCDC93 适用: 人, 大鼠, 犬, 猴, 小鼠 WB 宿主: 小鼠 Monoclonal 2A4 unconjugated
anti-Coiled-Coil Domain Containing 93 (CCDC93) (AA 531-631) antibodyCCDC93 适用: 大鼠 IF (cc), IF (p), ELISA, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))
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别名
- CCDC93
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背景
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Synonyms: CCDC 93, Coiled-coil domain containing 93, FLJ10996, FLJ25197, MGC13033, CCD93_HUMAN.
Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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 related to mutations in the ALMS1 gene.
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基因ID
- 54520
抗原
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