EML1 抗体
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- 抗原 See all EML1 抗体
- EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))
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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 EML1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 交叉反应
- 人, 小鼠
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human EML1. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product EML1 Primary Antibody
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anti-Echinoderm Microtubule Associated Protein Like 1 (EML1) (C-Term) antibody
EML1 适用: 人, 小鼠, 大鼠, 猴 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Echinoderm Microtubule Associated Protein Like 1 (EML1) (AA 1-99) antibodyEML1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 5G3 unconjugated
anti-Echinoderm Microtubule Associated Protein Like 1 (EML1) (C-Term) antibodyEML1 适用: 人, 小鼠, 大鼠, 犬, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Echinoderm Microtubule Associated Protein Like 1 (EML1) (C-Term) antibodyEML1 适用: 人, 小鼠, 大鼠, 犬, 兔, Cow, 豚鼠, 马, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: Mouse brain , A549
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.62 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): 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
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))
- 别名
- EMAP like 1 (EML1 产品)
- 背景
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Synonyms: EMAP like 1 , BH , ELP79 , EMAP , EMAPL , HuEMAP
Background: Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]
- 分子量
- 90 kDa
- 基因ID
- 2009
- UniProt
- O00423
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