Rho-related GTP-binding protein 抗体
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- 抗原 See all Rho-related GTP-binding protein (RhO (pan)) 抗体
- Rho-related GTP-binding protein (RhO (pan))
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适用
- 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 Rho-related GTP-binding protein antibody is un-conjugated
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应用范围
- Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- A synthetic peptide of human RHO (NP_000530.1).
- 亚型
- IgG
- Top Product
- Discover our top product RhO (pan) Primary Antibody
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anti-Rho-related GTP-binding protein (RhO (pan)) (C-Term) antibody
RhO (pan) 适用: 人, 小鼠, 大鼠 ELISA, WB, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) antibodyRhO (pan) 适用: Cow WB, ICC, IF, IHC (p) 宿主: 小鼠 Monoclonal B630 unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) antibodyRhO (pan) 适用: Cow WB, IF, IHC (p) 宿主: 小鼠 Monoclonal A531 unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) (C-Term) antibodyRhO (pan) 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) antibodyRhO (pan) 适用: 人 WB, IHC 宿主: 兔 Monoclonal unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) antibodyRhO (pan) 适用: Cow WB, IHC 宿主: 小鼠 Monoclonal 1D4 unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) (Internal Region) antibodyRhO (pan) 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) antibodyRhO (pan) 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Rho-related GTP-binding protein (RhO (pan)) (AA 62-93) antibodyRhO (pan) 适用: 斑马鱼 WB 宿主: 兔 Polyclonal RB52315 unconjugated
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- 应用备注
- IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- Rho-related GTP-binding protein (RhO (pan))
- 别名
- RHO (RhO (pan) 产品)
- 背景
- Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.
- 基因ID
- 6010
- UniProt
- P08100
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