LHX4 抗体 (Middle Region)
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- 抗原 See all LHX4 抗体
- LHX4 (LIM Homeobox 4 (LHX4))
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抗原表位
- Middle Region
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适用
- 人, 小鼠, 大鼠, Cow, 犬, 山羊, 豚鼠, 马
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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 LHX4 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- GSFSMDGTGQ SYQDLRDGSP YGIPQSPSSI SSLPSHAPLL NGLDYTVDSN
- 预测反应
- Cow: 100%, Dog: 100%, Goat: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rat: 100%
- 产品特性
- This is a rabbit polyclonal antibody against LHX4. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human LHX4
- Top Product
- Discover our top product LHX4 Primary Antibody
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 390 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 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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- 抗原
- LHX4 (LIM Homeobox 4 (LHX4))
- 别名
- LHX4 (LHX4 产品)
- 背景
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LHX4 is a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects.This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects. An alternative splice variant has been described but its biological nature has not been determined. 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: Gsh-4, Gsh4, CPHD4
Protein Interaction Partner: FDX1L, LONRF1, TXNDC5, SNRNP25, CHCHD2, ORC6, USP2, SH2D1A, LDB2, SSX1, ISL1, IFT172,
Protein Size: 390 - 分子量
- 43 kDa
- 基因ID
- 89884
- NCBI登录号
- NM_033343, NP_203129
- UniProt
- P53776
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