LCA5 抗体 (N-Term)
(1 reference)Quick Overview for LCA5 抗体 (N-Term) (ABIN2785382)
抗原
See all LCA5 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- N-Term
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序列
- FSLQKLKEIS EARHLPERDD LAKKLVSAEL KLDDTERRIK ELSKNLELST
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预测反应
- Cow: 92%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%
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产品特性
- This is a rabbit polyclonal antibody against LCA5. It was validated on Western Blot using a cell lysate as a positive control.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the N terminal region of human LCA5
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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 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
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说明
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Antigen size: 697 AA
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- Lot specific
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缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freeze-thaw cycles.
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储存条件
- -20 °C
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储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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: "Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis." in: Molecular vision, Vol. 14, pp. 481-6, (2008) (PubMed).
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: "Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis." in: Molecular vision, Vol. 14, pp. 481-6, (2008) (PubMed).
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- LCA5 (Leber Congenital Amaurosis 5 (LCA5))
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别名
- LCA5
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背景
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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.
Alias Symbols: C6orf152
Protein Interaction Partner: TXLNA, RCOR3, SRPK2,
Protein Size: 697 -
分子量
- 80 kDa
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基因ID
- 167691
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NCBI登录号
- NM_181714, NP_859065
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UniProt
- Q86VQ0
抗原
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