Aristaless Related Homeobox (ARX) (Middle Region) Peptide
ARX
适用: 人
宿主: 合成
BP, WB
产品编号 ABIN973474
发货至:
中国
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Quick Overview for Aristaless Related Homeobox (ARX) (Middle Region) Peptide (ABIN973474)
抗原
Arx (ARX)
(Aristaless Related Homeobox (ARX))
宿主
人
资源
合成
应用范围
Blocking Peptide (BP), Western Blotting (WB)
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蛋白结构域
- Middle Region
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产品特性
- This is a synthetic peptide designed for use in combination with anti-ARX antibody (Catalog #: ARP31598_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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纯化方法
- Purified
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应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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浓度
- 1 mg/mL
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缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
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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 longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Arx (ARX) (Aristaless Related Homeobox (ARX))
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背景
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ARX gene is a homeobox-containing gene expressed during development. The expressed protein ARX contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy.This gene is a homeobox-containing gene expressed during development. The expressed protein contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRXS1, PRTS, CT121, EIEE1, MRX76, MRX87
Protein Size: 562 -
分子量
- 58 kDa
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基因ID
- 170302
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NCBI登录号
- NM_139058, NP_620689
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UniProt
- Q96QS3
抗原
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