FANCG 抗体 (pSer383) (AbBy Fluor® 350)
Quick Overview for FANCG 抗体 (pSer383) (AbBy Fluor® 350) (ABIN875881)
抗原
See all FANCG 抗体适用
宿主
克隆类型
标记
应用范围
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    - 
                                            抗原表位
- pSer383
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                                            预测反应
- Human,Mouse,Rat
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                                            纯化方法
- Purified by Protein A.
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                                            免疫原
- KLH conjugated synthetic phosphopeptide derived from human FANCG around the phosphorylation site of Ser383
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                                            亚型
- IgG
 
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                                            应用备注
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                        IF(IHC-P) 1:50-200
 IF(IHC-F) 1:50-200
 IF(ICC) 1:50-200
- 
                                            限制
- 仅限研究用
 
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    - 
                                            状态
- Liquid
- 
                                            浓度
- 1 μg/μL
- 
                                            缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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                                            储存液
- ProClin
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                                            注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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                                            储存条件
- -20 °C
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                                            储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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                                            有效期
- 12 months
 
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    - FANCG (Fanconi Anemia Complementation Group G (FANCG))
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                                            别名
- FANCG
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                                            背景
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                        Synonyms: FANCG phospho S383, p-FANCG phospho S383, DNA repair protein XRCC9, DNA-repair protein XRCC9, FAG, Fanconi anaemia complementation group G, Protein FACG, X ray repair, complementing defective, in Chinese hamster cells 9, XRCC9. Background: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified. 
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                                            基因ID
- 2189
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                                            途径
- DNA Damage Repair
 抗原
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