EML1 抗体 (C-Term)
Quick Overview for EML1 抗体 (C-Term) (ABIN2784635)
抗原
See all EML1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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序列
- YPCSQFRAPS HIYGGHSSHV TNVDFLCEDS HLISTGGKDT SIMQWRVI
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预测反应
- Cow: 93%, Dog: 100%, Guinea Pig: 92%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 92%, Rat: 100%, Zebrafish: 93%
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产品特性
- This is a rabbit polyclonal antibody against EML1. It was validated on Western Blot using a cell lysate as a positive control.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the C terminal region of human EML1
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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
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
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说明
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Antigen size: 834 AA
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- Lot specific
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缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freeze-thaw cycles.
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储存条件
- -20 °C
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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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- EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))
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别名
- EML1
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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. 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.
Alias Symbols: ELP79, EMAP, EMAPL, FLJ45033, HuEMAP
Protein Interaction Partner: TUBB3, TUBA1B, ISG20L2, DCUN1D1, GRID1, GRID2,
Protein Size: 834 -
分子量
- 92 kDa
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基因ID
- 2009
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NCBI登录号
- NM_001008707, NP_001008707
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UniProt
- O00423
抗原
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