AHI1 抗体 (AA 1-12)
Quick Overview for AHI1 抗体 (AA 1-12) (ABIN1885582)
抗原
See all AHI1 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 1-12
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Synthetic peptide contain a sequence corresponding to a region within amino acids 1 and 12 of Jouberin
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anti-Abelson Helper Integration Site 1 (AHI1) (AA 1-609) antibody
AHI1 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (AA 1-213) antibodyAHI1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (AA 1-609) antibodyAHI1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (C-Term) antibodyAHI1 适用: 小鼠 WB, IHC, IP, ICC, IF 宿主: 小鼠 Monoclonal F-tag-01 unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (AA 389-422) antibodyAHI1 适用: 人 WB 宿主: 兔 Polyclonal RB53478 unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (AA 1-42) antibodyAHI1 适用: 人 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (N-Term) antibodyAHI1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (AA 671-720) antibodyAHI1 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Bat, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Abelson Helper Integration Site 1 (AHI1) (C-Term) antibodyAHI1 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- AHI1 (Abelson Helper Integration Site 1 (AHI1))
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别名
- Jouberin
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背景
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This gene is apparently required for both cerebellar and cortical development in humans.This gene mutations cause specific forms of Joubert syndrome-related disorders.Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci.Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq]
Synonyms: ORF1, AHI-1, JBTS3, FLJ14023, FLJ20069, dJ71N10.1, DKFZp686J1653 -
分子量
- 137 kDa
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基因ID
- 54806
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NCBI登录号
- NP_060121, NM_017651
抗原
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