Nyctalopin 抗体 (AA 139-189)
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Quick Overview for Nyctalopin 抗体 (AA 139-189) (ABIN8123495)
抗原
See all Nyctalopin (NYX) 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 139-189
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原理
- NYX Antibody
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特异性
- This antibody detects endogenous levels of NYX at Human/Mouse
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from human NYX AA range: 139-189
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亚型
- IgG
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anti-Nyctalopin (NYX) (AA 282-481) antibody
NYX 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Nyctalopin (NYX) (AA 53-80), (N-Term) antibodyNYX 适用: 人 WB 宿主: 兔 Polyclonal RB23621 unconjugated
anti-Nyctalopin (NYX) (AA 59-89), (N-Term) antibodyNYX 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:500-2000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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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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储存条件
- -20 °C
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储存方法
- Store at -20°C/1 year
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有效期
- 12 months
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- Nyctalopin (NYX)
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别名
- NYX
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背景
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Background: The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008],
Gene Name: NYX CLRP
Protein Name: NYX
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基因ID
- 60506
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UniProt
- Q9GZU5
抗原
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