Arylsulfatase E 抗体 (Middle Region)
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- 抗原 See all Arylsulfatase E (ARSE) 抗体
- Arylsulfatase E (ARSE)
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抗原表位
- Middle Region
- 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 Arylsulfatase E antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS
- 预测反应
- Human: 100%
- 产品特性
- This is a rabbit polyclonal antibody against ARSE. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human ARSE
- Top Product
- Discover our top product ARSE Primary Antibody
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 589 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- Arylsulfatase E (ARSE)
- 别名
- ARSE (ARSE 产品)
- 别名
- ASE antibody, CDPX antibody, CDPX1 antibody, CDPXR antibody, ARSE antibody, MGC155058 antibody, arylsulfatase E (chondrodysplasia punctata 1) antibody, arylsulfatase E antibody, ARSE antibody, Arse antibody
- 背景
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Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-170 AC005295.1 87561-87730 c 171-744 AK223183.1 1-574 745-2036 AK223199.1 542-1833 2037-2220 AW779826.1 1-184 c
Alias Symbols: CDPX, CDPX1, CDPXR, MGC163310, ASE
Protein Interaction Partner: COQ6, TMEM259, TNK2, NDN,
Protein Size: 589 - 分子量
- 62 kDa
- 基因ID
- 415
- NCBI登录号
- NM_000047, NP_000038
- UniProt
- P51690
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