BEND2 抗体 (AbBy Fluor® 555)
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- 抗原 See all BEND2 抗体
- BEND2 (BEN Domain Containing 2 (BEND2))
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适用
- 人
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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 BEND2 antibody is conjugated to AbBy Fluor® 555
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human BEND2/CXorf56
- 亚型
- IgG
- Top Product
- Discover our top product BEND2 Primary Antibody
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anti-BEN Domain Containing 2 (BEND2) (AA 1-799) antibody
BEND2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-BEN Domain Containing 2 (BEND2) (C-Term) antibodyBEND2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-BEN Domain Containing 2 (BEND2) (AA 611-660) antibodyBEND2 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- 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
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- BEND2 (BEN Domain Containing 2 (BEND2))
- 别名
- BEND2 (BEND2 产品)
- 别名
- CXorf20 antibody, BEN domain containing 2 antibody, BEND2 antibody
- 背景
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Synonyms: BEN domain-containing protein 2, BEN domain containing 2, BEND 2, BEND2, BEND-2, Chromosome X open reading frame 20, MGC33653, BEND2_HUMAN, CXorf56.
Background: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates proteinDNA and proteinprotein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
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