EHMT1 抗体 (AA 25-75)
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- 抗原 See all EHMT1 抗体
- EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))
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抗原表位
- AA 25-75
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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 EHMT1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
- 原理
- Rabbit anti-EHMT1 Antibody, Affinity Purified
- 纯化方法
- Affinity Purified
- 免疫原
- between AA 25 and 75
- 亚型
- IgG
- Top Product
- Discover our top product EHMT1 Primary Antibody
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- 应用备注
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IHC: 1:100 - 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.
IP: 2 - 5 μg/mg lysate
WB: 1:2,000 - 1:10,000
- 限制
- 仅限研究用
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- 浓度
- 200 μg/mL
- 缓冲液
- Tris-buffered Saline containing 0.1 % BSA and 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
- EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))
- 别名
- EHMT1 (EHMT1 产品)
- 别名
- EUHMTASE1 antibody, Eu-HMTase1 antibody, FP13812 antibody, GLP antibody, GLP1 antibody, KMT1D antibody, bA188C12.1 antibody, EHMT1 antibody, G9a antibody, 9230102N17Rik antibody, D330003E03 antibody, mKIAA1876 antibody, bZ1O1.6 antibody, si:rp71-1o1.6 antibody, zgc:136244 antibody, euchromatic histone lysine methyltransferase 1 antibody, histone-lysine N-methyltransferase EHMT2 antibody, euchromatic histone-lysine N-methyltransferase 1 antibody, euchromatic histone methyltransferase 1 antibody, euchromatic histone-lysine N-methyltransferase 1a antibody, EHMT1 antibody, Ehmt1 antibody, LOC100121084 antibody, ehmt1 antibody, ehmt1a antibody
- 背景
- Background: Euchromatic histone-lysine N-methyltransferase 1 (EHMT1) is a histone methyltransferase that catalyzes the methylation of lysine-9 of histone H3 (H3-K9). H3-K9 histone methylation is restricted to euchromatin and functions to epigenetically silence gene transcription. Loss of function mutations in EHMT1 cause the 9q34 subtelomeric deletion syndrome, a syndrome characterized by severe mental retardation, hypotonia, brachy(micro)cephaly, heart defects, and distinct facial anomalies.
- 基因ID
- 79813
- NCBI登录号
- NP_079033
- UniProt
- Q9H9B1
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