EIF4H 抗体 (C-Term)
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- 抗原 See all EIF4H 抗体
- EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))
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抗原表位
- C-Term
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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 EIF4H antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- EIF4 H antibody was raised against the C terminal of EIF4
- 纯化方法
- Affinity purified
- 免疫原
- EIF4 H antibody was raised using the C terminal of EIF4 corresponding to a region with amino acids TEEERAQRPRLQLKPRTVATPLNQVANPNSAIFGGARPREEVVQKEQE
- Top Product
- Discover our top product EIF4H Primary Antibody
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- 应用备注
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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EIF4H Blocking Peptide, catalog no. 33R-9032, is also available for use as a blocking control in assays to test for specificity of this EIF4H antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of EIF0 antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 抗原
- EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))
- 别名
- EIF4H (EIF4H 产品)
- 别名
- wscr1 antibody, wbscr1 antibody, WBSCR1 antibody, Wbscr1 antibody, WSCR1 antibody, eIF-4H antibody, AU018978 antibody, D5Ertd355e antibody, E430026L18Rik antibody, Ef4h antibody, Wscr1 antibody, mKIAA0038 antibody, zgc:77282 antibody, eukaryotic translation initiation factor 4H antibody, eukaryotic translation initiation factor 4H L homeolog antibody, eukaryotic translation initiation factor 4h antibody, transaltion initiation factor antibody, Eukaryotic translation initiation factor 4H antibody, eif4h antibody, eif4h.L antibody, EIF4H antibody, Eif4h antibody, LOC733087 antibody, SJAG_03433 antibody, MGYG_07815 antibody, Tsp_06589 antibody, if4h antibody
- 背景
- EIF4H is one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
- 分子量
- 27 kDa (MW of target protein)
- 途径
- SARS-CoV-2 Protein Interactome
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