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SmcX Monoclonal Antibody
商品货号: PLA005152
适 应 性: 人,小鼠,大鼠,牛,狗
WB IF
¥600元
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MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: KDM5C
  • 蛋白名称: Lysine-specific demethylase 5C
  • Human_gene_id: 8242
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=8242
  • Human_swiss_prot_no: P41229
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P41229/entry
  • Mouse_gene_id: 20591
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20591
  • Mouse_swiss_prot_no: P41230
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P41230
  • 特异性: SmcX Monoclonal Antibody detects endogenous levels of SmcX protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: WB 1:1000 - 1:2000. IF 1:100 - 1:500. Not yet tested in other applications.
  • 纯化工艺: Affinity purification
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: KDM5C; DXS1272E; JARID1C; SMCX; XE169; Lysine-specific demethylase 5C; Histone demethylase JARID1C; Jumonji/ARID domain-containing protein 1C; Protein SmcX; Protein Xe169
  • 功能: cofactor:Alpha-ketoglutarate.,cofactor:Fe(2+).,disease:Defects in KDM5C are a cause of X-linked mental retardation (XLMR) [MIM:300534]. Mental retardation is usually defined as cognitive impairment with an IQ less than 70. Etiologically, mental retardation is a very heterogeneous condition that involves environmental, stochastic and/or genetic factors.,domain:Both the JmjC domain and the JmjN domain are required for enzymatic activity.,domain:The first PHD-type zinc finger domain recognizes and binds H3-K9Me3.,function:Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. Participates in transcriptional repression of neuronal genes by recruiting histone deacetylases and REST at neuron-restrictive silencer elements.,miscellaneous:Escapes X-inactivation.,similarity:Belongs to the JARID1 histone demethylase family.,similarity:Contains 1 ARID domain.,similarity:Contains 1 JmjC domain.,similarity:Contains 1 JmjN domain.,similarity:Contains 2 PHD-type zinc fingers.,subunit:Part of two distinct complexes, one containing E2F6, and the other containing REST.,tissue specificity:Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.,
  • 相关产品: YM1201,YM1096,RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus .
  • 组织表达: Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.
  • 科研货号: PLA005152
SmcX Monoclonal Antibody
Catalog No PLA005152
Product information
  • 发货日期: 7
  • 基因名称: KDM5C
  • 蛋白名称: Lysine-specific demethylase 5C
  • Human_gene_id: 8242
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=8242
  • Human_swiss_prot_no: P41229
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P41229/entry
  • Mouse_gene_id: 20591
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20591
  • Mouse_swiss_prot_no: P41230
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P41230
  • 特异性: SmcX Monoclonal Antibody detects endogenous levels of SmcX protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: WB 1:1000 - 1:2000. IF 1:100 - 1:500. Not yet tested in other applications.
  • 纯化工艺: Affinity purification
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: KDM5C; DXS1272E; JARID1C; SMCX; XE169; Lysine-specific demethylase 5C; Histone demethylase JARID1C; Jumonji/ARID domain-containing protein 1C; Protein SmcX; Protein Xe169
  • 功能: cofactor:Alpha-ketoglutarate.,cofactor:Fe(2+).,disease:Defects in KDM5C are a cause of X-linked mental retardation (XLMR) [MIM:300534]. Mental retardation is usually defined as cognitive impairment with an IQ less than 70. Etiologically, mental retardation is a very heterogeneous condition that involves environmental, stochastic and/or genetic factors.,domain:Both the JmjC domain and the JmjN domain are required for enzymatic activity.,domain:The first PHD-type zinc finger domain recognizes and binds H3-K9Me3.,function:Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. Participates in transcriptional repression of neuronal genes by recruiting histone deacetylases and REST at neuron-restrictive silencer elements.,miscellaneous:Escapes X-inactivation.,similarity:Belongs to the JARID1 histone demethylase family.,similarity:Contains 1 ARID domain.,similarity:Contains 1 JmjC domain.,similarity:Contains 1 JmjN domain.,similarity:Contains 2 PHD-type zinc fingers.,subunit:Part of two distinct complexes, one containing E2F6, and the other containing REST.,tissue specificity:Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.,
  • 相关产品: YM1201,YM1096,RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus .
  • 组织表达: Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.
  • 科研货号: PLA005152
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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