EFR3B 抗体 (AA 21-120) (Biotin)
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- 抗原 See all EFR3B products
- EFR3B (EFR3 Homolog B (EFR3B))
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抗原表位
- AA 21-120
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适用
- 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 EFR3B antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 小鼠, 大鼠
- 预测反应
- Human,Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human EFR3B
- 亚型
- IgG
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anti-EFR3 Homolog B (EFR3B) (AA 1-298) antibody
EFR3B 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 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.
- 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
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- EFR3B (EFR3 Homolog B (EFR3B))
- 别名
- EFR3B (EFR3B 产品)
- 别名
- KIAA0953 antibody, AI852640 antibody, C030014M07Rik antibody, mKIAA0953 antibody, efr3b antibody, si:ch211-203k16.1 antibody, si:ch211-215m21.18 antibody, si:dkeyp-70e6.6 antibody, EFR3 homolog B antibody, EFR3 homolog Bb (S. cerevisiae) antibody, EFR3B antibody, Efr3b antibody, efr3bb antibody
- 背景
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Synonyms: EFR3B, EFR3B_HUMAN, KIAA0953, Protein EFR3 homolog B.
Background: EFR3B (EFR3 homolog B) is an 817 amino acid protein that exists as three alternatively spliced isoforms and belongs to the EFR3 family. The gene encoding EFR3B maps to human chromosome 2p23.3 and mouse chromosome 12 A1.1. Human chromosome 2 is the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr_ syndrome, is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- 基因ID
- 22979
- UniProt
- Q9Y2G0
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