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OTX2 抗体 (AA 1-204)
OTX2
适用: 人
WB
宿主: 兔
Polyclonal
unconjugated
OTX2抗体详情
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抗原
See all OTX2 抗体
OTX2
(Orthodenticle Homeobox 2 (OTX2))
抗原表位
All epitopes for OTX2 抗体
AA 1-204
适用
All reactivities for OTX2 抗体
人
宿主
All hosts for OTX2 抗体
兔
克隆类型
All clonalities for OTX2 抗体
多克隆
标记
All conjugates for OTX2 抗体
This OTX2 antibody is un-conjugated
应用范围
All applications for OTX2 抗体
Western Blotting (WB)
纯化方法
Protein A Chromatography
免疫原
A partial length recombinant Otx2 protein (amino acids 1-204) was used as the immunogen for this antibody.
亚型
IgG
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Discover our top product OTX2 Primary Antibody
Alternatives
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anti-Orthodenticle Homeobox 2 (OTX2) (N-Term) antibody
OTX2
适用: 人, 大鼠, 小鼠, 斑马鱼, 兔, Cow, 绵羊, 犬, 马, 豚鼠
WB, IHC
宿主: 兔
Polyclonal
unconjugated
anti-Orthodenticle Homeobox 2 (OTX2) (AA 86-135) antibody
OTX2
适用: 人, 大鼠, 小鼠, 斑马鱼, 兔, Cow, 绵羊, 犬, 马, 豚鼠, Pig, Bat, Hamster, 小鸡
WB
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
WB: 2-4 μg/mL
限制
仅限研究用
贮存及处理
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浓度
0.5 mg/mL
缓冲液
PBS containing 0.05 % BSA, PH 7.4
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
4 °C/-20 °C
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.
OTX2目标详情
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抗原
OTX2
(Orthodenticle Homeobox 2 (OTX2))
别名
Otx2 (OTX2 产品 )
别名
CPHD6 antibody, MCOPS5 antibody, E130306E05Rik antibody, id:ibd2915 antibody, zOtx2 antibody, zgc:136535 antibody, zotx-2 antibody, Xotx-2 antibody, Xotx2 antibody, otx-2 antibody, otx2 antibody, orthodenticle homeobox 2 antibody, orthodenticle homeobox 2 S homeolog antibody, orthodenticle homeobox 2 L homeolog antibody, OTX2 antibody, Otx2 antibody, otx2 antibody, otx2.S antibody, otx2.L antibody
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.
分子量
32 kDa
基因ID
5015
UniProt
P32243
途径
Dopaminergic Neurogenesis
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