EML1 抗体 (AA 772-834)
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- 抗原 See all EML1 抗体
- EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))
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抗原表位
- AA 772-834
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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)
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Synthetic peptide contain a sequence corresponding to a region within amino acids 772 and 834 of EML1
- 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
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Suggested dilutions:
Western blotting: 1.500-1.3000 - 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- 1 x PBS, 1 % BSA, 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- 抗原
- EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))
- 别名
- EML1 (EML1 产品)
- 别名
- ELP79 antibody, EMAP antibody, EMAPL antibody, HuEMAP antibody, EML1 antibody, MGC108311 antibody, wu:fj01a06 antibody, zgc:153105 antibody, 1110008N23Rik antibody, A930030P13Rik antibody, AA171013 antibody, AI847476 antibody, AI853955 antibody, echinoderm microtubule associated protein like 1 antibody, echinoderm microtubule associated protein like 1 S homeolog antibody, EML1 antibody, eml1.S antibody, eml1 antibody, Eml1 antibody
- 背景
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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
- 92 kDa
- 基因ID
- 2009
- NCBI登录号
- NM_001008707, NP_001008707
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