RBFA 抗体
Quick Overview for RBFA 抗体 (ABIN1385454)
抗原
See all RBFA 抗体适用
宿主
克隆类型
标记
应用范围
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    - 
                                            交叉反应
- 人, 小鼠, 大鼠
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                                            纯化方法
- Purified by Protein A.
- 
                                            免疫原
- KLH conjugated synthetic peptide derived from human RBFA
- 
                                            亚型
- IgG
 
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                                            应用备注
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                        WB 1:300-5000
 IHC-P 1:200-400
 IF(IHC-P) 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 
                                            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
- 4 °C,-20 °C
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                                            储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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                                            有效期
- 12 months
 
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    - RBFA (Ribosome Binding Factor A (RBFA))
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                                            别名
- RBFA
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                                            背景
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                        Synonyms: mitochondrial, C18orf25, Chromosome 18 open reading frame 22, HsT169, Hypothetical protein LOC79863, Putative ribosome binding factor A, mitochondrial precursor, Putative ribosome-binding factor A, rbfA, RBFA_HUMAN. Background: C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas. 
 抗原
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