Arylsulfatase A 抗体 (Middle Region)
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- 抗原 See all Arylsulfatase A (ARSA) 抗体
- Arylsulfatase A (ARSA)
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抗原表位
- Middle Region
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适用
- 人, 小鼠, 大鼠, 兔, Cow, 马, 犬, Pig
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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 A antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- KQLQLLKAQL DAAVTFGPSQ VARGEDPALQ ICCHPGCTPR PACCHCPDPH
- 预测反应
- Cow: 79%, Dog: 92%, Horse: 92%, Human: 100%, Mouse: 86%, Pig: 92%, Rabbit: 79%, Rat: 85%
- 产品特性
- This is a rabbit polyclonal antibody against ARSA. 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 ARSA
- Top Product
- Discover our top product ARSA 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: 507 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 A (ARSA)
- 别名
- ARSA (ARSA 产品)
- 别名
- ARSA antibody, zgc:101575 antibody, arsa antibody, AS-A antibody, ASA antibody, AW212749 antibody, As-2 antibody, As2 antibody, TISP73 antibody, MLD antibody, mld antibody, arylsulfatase A antibody, arylsulfatase antibody, arylsulfatase A, gene 1 S homeolog antibody, ARSA antibody, arsa antibody, arsA antibody, RB6599 antibody, Arsa antibody, arsa.1.S antibody
- 背景
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ARSA hydrolyzes cerebroside sulfate. Defects in ARSA are a cause of leukodystrophy metachromatic (MLD).The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene.
Alias Symbols: MLD
Protein Interaction Partner: TRIP13, PPIC, CETN2, CLEC4G, ARSA, GAL3ST1, BMPR2, CTSL,
Protein Size: 507 - 分子量
- 52 kDa
- 基因ID
- 410
- NCBI登录号
- NM_001085427, NP_001078896
- UniProt
- P15289
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