LIM Homeobox 3 (LHX3) (Middle Region) Peptide
LHX3
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all LHX3 products
- LHX3 (LIM Homeobox 3 (LHX3))
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-LHX3 antibody (Catalog #: ARP33644_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.
- 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.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- LHX3 (LIM Homeobox 3 (LHX3))
- 别名
- CPHD3 Peptide, LIM3 Peptide, M2-LHX3 Peptide, lim3 Peptide, LIM-3 Peptide, xlim-3 Peptide, lim-3 Peptide, Lim3 Peptide, P-LIM Peptide, mLIM3 Peptide, mLim-3 Peptide, lim homeobox 3 Peptide, LIM/homeobox protein Lhx3 Peptide, LIM homeobox 3 Peptide, LIM homeobox 3 L homeolog Peptide, LIM homeobox protein 3 Peptide, LOC662120 Peptide, LOC100224079 Peptide, LHX3 Peptide, Lhx3 Peptide, lhx3 Peptide, lhx3.L Peptide
- 背景
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LHX3 encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. This gene encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. Two transcripts variants encoding distinct isoforms have been identified for this gene.
Alias Symbols: DKFZp762A2013, M2-LHX3, LIM3, CPHD3
Protein Interaction Partner: CITED2,IFT172,ISL1,ISL2,LDB1,RLIM,CITED2,IFT172,ISL1,ISL2,LHX1,LMX1A,RLIM
Protein Size: 402 - 分子量
- 44 kDa
- 基因ID
- 8022
- NCBI登录号
- NM_014564, NP_055379
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