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- 抗原 See all RBFA 抗体
- RBFA (Ribosome Binding Factor A (RBFA))
- 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 RBFA antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RBFA
- 亚型
- IgG
- Top Product
- Discover our top product RBFA Primary Antibody
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anti-Ribosome Binding Factor A (RBFA) (AA 201-343) antibody
RBFA 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ribosome Binding Factor A (RBFA) (AA 1-343) antibodyRBFA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Ribosome Binding Factor A (RBFA) (C-Term) antibodyRBFA 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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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
- 注意事项
- This product contains ProClin: 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
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- RBFA (Ribosome Binding Factor A (RBFA))
- 别名
- RBFA (RBFA 产品)
- 别名
- C18orf22 antibody, HsT169 antibody, 1110032A13Rik antibody, AI595940 antibody, RGD1311910 antibody, zgc:162590 antibody, ribosome binding factor A antibody, RBFA antibody, Rbfa antibody, rbfa antibody
- 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.
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