MYT1L 抗体 (AA 195-825)
The 兔 多克隆 anti-MYT1L antibody is suitable to detect MYT1L in samples from 人. It has been validated for WB, ELISA, IF 和 FACS.
产品编号 ABIN7871706
发货至:
中国
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Quick Overview for MYT1L 抗体 (AA 195-825) (ABIN7871706)
抗原
See all MYT1L 抗体
MYT1L
(Myelin Transcription Factor 1-Like (MYT1L))
适用
人
宿主
兔
克隆类型
多克隆
标记
This MYT1L antibody is un-conjugated
应用范围
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
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抗原表位
- AA 195-825
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原理
- MYT1L Antibody / Myelin transcription factor 1-like protein
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纯化方法
- Antigen affinity purified
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免疫原
- An E.coli-derived human recombinant protein (D195-K825) was used as the immunogen for the MYT1L antibody.
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亚型
- IgG
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anti-Myelin Transcription Factor 1-Like (MYT1L) (AA 301-410) antibody
MYT1L 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2G5 unconjugated
anti-Myelin Transcription Factor 1-Like (MYT1L) (C-Term) antibodyMYT1L 适用: 人, 小鼠, 大鼠 WB, IF, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the MYT1L antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the MYT1L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- MYT1L (Myelin Transcription Factor 1-Like (MYT1L))
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别名
- MYT1L
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背景
- Myelin transcription factor 1 like is a protein that in humans is encoded by the MYT1L gene. This gene encodes a member of the zinc finger superfamily of transcription factors whose expression, thus far, has been found only in neuronal tissues. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with an autosomal dominant form of cognitive disability and with autism spectrum disorder. Alternative splicing results in multiple variants.
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UniProt
- Q9UL68
抗原
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