TMEM43 抗体 (AA 195-223)
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- 抗原 See all TMEM43 抗体
- TMEM43 (Transmembrane Protein 43 (TMEM43))
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抗原表位
- AA 195-223
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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 TMEM43 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- M, Rat
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This TMEM43 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 195-223 amino acids from the Central region of human TMEM43.
- 克隆位点
- RB32139
- 亚型
- Ig Fraction
- Top Product
- Discover our top product TMEM43 Primary Antibody
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anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibody
TMEM43 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 178-312) antibodyTMEM43 适用: 人 IHC, WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) antibodyTMEM43 适用: 人, 小鼠 IHC, WB 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibodyTMEM43 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB: 1:1000. IHC-P: 1:10~50
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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
- TMEM43 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
- 有效期
- 6 months
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- 抗原
- TMEM43 (Transmembrane Protein 43 (TMEM43))
- 别名
- TMEM43 (TMEM43 产品)
- 别名
- zgc:85946 antibody, ARVC5 antibody, ARVD5 antibody, EDMD7 antibody, LUMA antibody, 1200015A22Rik antibody, transmembrane protein 43 antibody, TMEM43 antibody, tmem43 antibody, Tmem43 antibody
- 背景
- This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC.
- 分子量
- 44876
- 基因ID
- 79188
- NCBI登录号
- NP_077310
- UniProt
- Q9BTV4
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