Distal-Less Homeobox 5 (DLX5) Peptide
DLX5
适用: 人
宿主: 合成
BP, IHC, WB
Quick Overview for Distal-Less Homeobox 5 (DLX5) Peptide (ABIN975853)
抗原
DLX5
(Distal-Less Homeobox 5 (DLX5))
宿主
人
资源
合成
应用范围
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
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产品特性
- This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP32867_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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Distal-Less Homeobox 5 (DLX5) peptide
DLX5 适用: 人, 小鼠, 大鼠, Cow 宿主: 合成 BP, Imm
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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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- DLX5 (Distal-Less Homeobox 5 (DLX5))
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背景
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DLX5 is a member of a homeobox transcription factor family. DLX5 may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.
Alias Symbols: SHFM1D
Protein Interaction Partner: MAGED1,MSX2,NCOA2,SOX10,SOX8,SPEN,DLX2,DLX5,HOXC8,MSX1,MSX2
Protein Size: 289 -
分子量
- 31 kDa
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基因ID
- 1749
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NCBI登录号
- NM_005221, NP_005212
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UniProt
- P56178
抗原
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