OTX2 抗体 (AA 1-204)
Quick Overview for OTX2 抗体 (AA 1-204) (ABIN5027412)
抗原
See all OTX2 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 1-204
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纯化方法
- Protein A Chromatography
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免疫原
- A partial length recombinant Otx2 protein (amino acids 1-204) was used as the immunogen for this antibody.
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亚型
- IgG
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anti-Orthodenticle Homeobox 2 (OTX2) antibody
OTX2 适用: 人 WB, ELISA, IHC, FACS, ICC 宿主: 小鼠 Monoclonal 1H12C4B5 unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (N-Term) antibodyOTX2 适用: 人, 大鼠, 小鼠, 斑马鱼, 犬, 绵羊, 兔, 马, Cow, 豚鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) antibodyOTX2 适用: 大鼠, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 1-297) antibodyOTX2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 86-135) antibodyOTX2 适用: 人, 大鼠, 小鼠, 斑马鱼, 犬, 绵羊, 兔, 马, Cow, 豚鼠, Bat, Hamster, Pig, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 140-280) antibodyOTX2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) antibodyOTX2 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 261-289), (C-Term) antibodyOTX2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB17482 unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 261-289) antibodyOTX2 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (C-Term) antibodyOTX2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 2-4 μg/mL
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限制
- 仅限研究用
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浓度
- 0.5 mg/mL
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缓冲液
- PBS containing 0.05 % BSA, PH 7.4
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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
- 4 °C/-20 °C
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储存方法
- Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
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- OTX2 (Orthodenticle Homeobox 2 (OTX2))
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别名
- Otx2
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背景
- Otx2 encodes a transcription factor that plays a critical role in craniofacial development and anterior brain morphogenesis. Otx2 homologs in model organisms are expressed in a complex spatial, temporal, and gradient-specific manner that is required for correct antero-posterior patterning and craniofacial development. Otx2 mutations are associated with severe ocular phenotypes and central nervous system abnormalities such as seizures, short stature and developmental delay, CPHD (Combined Pituitary Hormone Deficiency), structural abnormalities of the pituitary gland and early onset retinal dystrophy.
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分子量
- 32 kDa
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基因ID
- 5015
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UniProt
- P32243
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途径
- Dopaminergic Neurogenesis
抗原
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