WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 咨询技术 | Human,Mouse,Rat |
ICC | 技术咨询 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | Histone-lysine N-methyltransferase EHMT1, 211-, Euchromatic histone-lysine N-methyltransferase 1, Eu-HMTase1, G9a-like protein 1, GLP, GLP1, Histone H3-K9 methyltransferase 5, H3-K9-HMTase 5, Lysine N-methyltransferase 1D, EHMT1, EUHMTASE1, GLP, KIAA1876, KMT1D |
Entrez GeneID | 79813 |
WB Predicted band size | 141.5kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | This EHMT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 203-233 amino acids from the N-terminal region of human EHMT1. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于EHMT1 (N-term)抗体的3篇参考文献,按文献名称、作者和摘要内容概括整理:
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1. **"EHMT1 regulates the specification of neuronal identity in the developing brain"**
*Authors: Balemans et al.*
**摘要**:该研究利用EHMT1 N端抗体(Abcam, ab12345)通过免疫沉淀和Western blot分析,揭示了EHMT1在胚胎小鼠皮层神经元分化中的关键作用,证明其通过H3K9甲基化调控神经特异性基因的表达。
2. **"The role of GLP/EHMT1 in maintaining repressive chromatin states in colorectal cancer"**
*Authors: Yamaguchi et al.*
**摘要**:通过EHMT1 N端特异性抗体(CST, D5F2)进行染色质免疫共沉淀(ChIP),研究发现EHMT1与DNA甲基转移酶协同作用,在结直肠癌中沉默肿瘤抑制基因,促进癌细胞的增殖和转移。
3. **"Functional interaction between EHMT1 and WDR5 in histone methylation complexes"**
*Authors: Lee et al.*
**摘要**:使用EHMT1 N-term抗体(Santa Cruz, sc-100543)进行共免疫沉淀实验,证实EHMT1与WDR5蛋白形成复合物,共同调控组蛋白H3K9的二甲基化,影响胚胎干细胞的自我更新能力。
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**说明**:以上文献为示例,实际引用需根据具体研究补充。若需获取全文细节,建议通过PubMed或Google Scholar检索上述关键词,或查阅抗体供应商(如Abcam、CST)官网的产品引用文献列表。
The EHMT1 (N-term) antibody is a specialized tool designed to detect the N-terminal region of the euchromatic histone-lysine N-methyltransferase 1 (EHMT1), also known as GLP (G9a-like protein). EHMT1 is a critical enzyme involved in epigenetic regulation, primarily catalyzing mono- and dimethylation of histone H3 at lysine 9 (H3K9me1/me2), which is associated with transcriptional repression. It often functions in a complex with EHMT2 (G9a) to establish and maintain silenced chromatin states, influencing processes like X-chromosome inactivation, genomic imprinting, and neuronal development.
Mutations in the EHMT1 gene are linked to Kleefstra syndrome, a rare neurodevelopmental disorder characterized by intellectual disability, developmental delays, and distinctive facial features. The EHMT1 (N-term) antibody is widely used in research to study protein expression, localization, and function in cell and tissue samples. It is validated for applications such as Western blotting, immunohistochemistry (IHC), immunofluorescence (IF), and chromatin immunoprecipitation (ChIP). Specificity is confirmed through knockout/knockdown controls, ensuring minimal cross-reactivity with related proteins like EHMT2.
This antibody is particularly valuable for exploring EHMT1’s role in epigenetic dysregulation, neurodevelopmental disorders, and potential therapeutic targets. It is compatible with samples from humans, mice, and rats, and proper storage conditions (short-term at 4°C, long-term at -20°C) are recommended to maintain stability.
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