CHD7 抗体 (AA 2025-2075)
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- 抗原 See all CHD7 抗体
- CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))
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抗原表位
- AA 2025-2075
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适用
- 人
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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 CHD7 antibody is un-conjugated
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应用范围
- Immunoprecipitation (IP)
- 原理
- Rabbit anti-CHD7 Antibody, Affinity Purified
- 纯化方法
- Affinity Purified
- 免疫原
- between AA 2025 and 2075
- 亚型
- IgG
- Top Product
- Discover our top product CHD7 Primary Antibody
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- 应用备注
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IP: 2 - 10 μg/mg lysate
WB: Not recommended. Use rabbit anti-CHD7 antibody ABIN7453314.
- 限制
- 仅限研究用
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- 浓度
- 1000 μg/mL
- 缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- 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.
- 储存条件
- 4 °C
- 有效期
- 12 months
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- 抗原
- CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))
- 别名
- CHD7 (CHD7 产品)
- 别名
- CHD7 antibody, fd19h06 antibody, si:ch211-197o6.2 antibody, wu:cegs2051 antibody, wu:fb37f10 antibody, wu:fb39h04 antibody, wu:fd19h06 antibody, HH5 antibody, IS3 antibody, KAL5 antibody, A730019I05Rik antibody, Cycn antibody, Cyn antibody, Dz antibody, Edy antibody, Flo antibody, GENA 47 antibody, GENA 60 antibody, Gena 52 antibody, Lda antibody, Mt antibody, Obt antibody, Todo antibody, WBE1 antibody, Whi antibody, metis antibody, chromodomain helicase DNA binding protein 7 L homeolog antibody, chromodomain helicase DNA binding protein 7 antibody, chd7.L antibody, CHD7 antibody, chd7 antibody, Chd7 antibody
- 背景
- Background: CHD7 is a member of the CHD (chromodomain-helicase-DNA-binding) family of proteins that interacts with nucleosomes and plays a role in chromatin remodeling to modulate transcription. The members of the CHD family of proteins possess 3 common structural and functional domains: a chromodomain (chromatin organization modifier), an SNF2-like helicase/ATPase domain, and a C-terminal DNA-binding domain. CHD7 is implicated to play a role in development. Mutations in CHD7 are associated with CHARGE syndrome, a multi-symptom syndrome characterized by congenital anomalies and malformations of the heart, inner ear, retina, and palate.
- 基因ID
- 55636
- NCBI登录号
- NP_060250
- UniProt
- Q9P2D1
- 途径
- Sensory Perception of Sound, Chromatin Binding
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