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- 抗原 See all LCA5 抗体
- LCA5 (Leber Congenital Amaurosis 5 (LCA5))
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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 LCA5 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- Antibody is purified by peptide affinity chromatography method.
- 免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LCA5.
- Top Product
- Discover our top product LCA5 Primary Antibody
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anti-Leber Congenital Amaurosis 5 (LCA5) antibody
LCA5 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Leber Congenital Amaurosis 5 (LCA5) (AA 101-400) antibodyLCA5 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Leber Congenital Amaurosis 5 (LCA5) (AA 201-250) antibodyLCA5 适用: 人, 大鼠, 犬, 豚鼠, 马, 兔, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Leber Congenital Amaurosis 5 (LCA5) (N-Term) antibodyLCA5 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, 兔, Cow WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- LCA5 antibody can be used for detection of LCA5 by ELISA at 1:1562500. LCA5 antibody can be used for detection of LCA5 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- 浓度
- 1 mg/mL
- 缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- 注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store LCA5 antibody at -20 °C.
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- 抗原
- LCA5 (Leber Congenital Amaurosis 5 (LCA5))
- 别名
- LCA5 (LCA5 产品)
- 别名
- C6orf152 antibody, RGD1308555 antibody, 4930431B11Rik antibody, 5730406O13Rik antibody, AV274874 antibody, ORF64 antibody, LCA5, lebercilin antibody, Leber congenital amaurosis 5 antibody, Leber congenital amaurosis 5 (human) antibody, LCA5 antibody, LOC787523 antibody, Lca5 antibody
- 背景
- LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.
- 分子量
- 80 kDa
- 基因ID
- 167691
- NCBI登录号
- NP_859065
- UniProt
- Q86VQ0
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