AHI1 抗体 (AA 1146-1196)
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- 抗原 See all AHI1 抗体
- AHI1 (Abelson Helper Integration Site 1 (AHI1))
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抗原表位
- AA 1146-1196
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This AHI1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunoprecipitation (IP)
- 原理
- Rabbit anti-AHI1 Antibody, Affinity Purified
- 纯化方法
- Affinity Purified
- 免疫原
- between AA 1146 and 1196
- 亚型
- IgG
- Top Product
- Discover our top product AHI1 Primary Antibody
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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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IP: 2 - 10 μg/mg lysate
WB: 1:2,000 - 1:10,000
- 限制
- 仅限研究用
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- 浓度
- 1000 μg/mL
- 缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- 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
- 有效期
- 12 months
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- 抗原
- AHI1 (Abelson Helper Integration Site 1 (AHI1))
- 别名
- AHI1 (AHI1 产品)
- 背景
- Background: Abelson helper integration site 1 (AHI1) is also known as jouberin. AHI1 is apparently required for both cerebellar and cortical development in humans. Mutations in AH1 cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci [taken from NCBI Entrez Gene (Gene ID: 55054)].
- 基因ID
- 54806
- NCBI登录号
- NP_001128302
- UniProt
- Q8N157
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