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- 抗原 See all RTEL1 抗体
- RTEL1 (Regulator of Telomere Elongation Helicase 1 (RTEL1))
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抗原表位
- AA 651-756
- 适用
- 人, 小鼠, 大鼠
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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 RTEL1 antibody is un-conjugated
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应用范围
- ELISA, Western Blotting (WB)
- 交叉反应 （详细）
- No cross reactivity with other proteins.
- 产品特性
- Rabbit IgG polyclonal antibody for RTEL1 detection. Tested with WB, Direct ELISA in Human,Mouse,Rat.
- 免疫原
- E. coli-derived human RTEL1 recombinant protein (Position: R651-M756).
- Top Product
- Discover our top product RTEL1 Primary Antibody
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anti-Regulator of Telomere Elongation Helicase 1 (RTEL1) (AA 975-1219) antibody
RTEL1 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Regulator of Telomere Elongation Helicase 1 (RTEL1) antibodyRTEL1 适用: 人, 小鼠 ELISA, WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Regulator of Telomere Elongation Helicase 1 (RTEL1) (N-Term) antibodyRTEL1 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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Recommended Detection Systems: Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ABIN921124) for Western blot.
Application Details: Western blot, 0.1-0.5 μg/mL
Direct ELISA, 0.1-0.5 μg/mL - 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
- 缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg NaN3.
- 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
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At -20°C for one year. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
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- 抗原
- RTEL1 (Regulator of Telomere Elongation Helicase 1 (RTEL1))
- 别名
- RTEL1 (RTEL1 产品)
- 背景
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Synonyms: Regulator of telomere elongation helicase 1
Background: The RTEL1 gene encodes a DNA helicase which functions in the stability, protection and elongation of telomeres and interacts with proteins in the shelterin complex known to protect telomeres during DNA replication. Mutations in this gene have been associated with dyskeratosis congenita and Hoyerall-Hreidarsson syndrome. Read-through transcription of this gene into the neighboring downstream gene, which encodes tumor necrosis factor receptor superfamily, member 6b, generates a non-coding transcript. Alternative splicing results in multiple transcript variants encoding different isoforms.
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