首页 > 抗体 > 一抗 > 其它 > WBS22 rabbit pAb
WBS22 rabbit pAb
商品货号: PLA009243
适 应 性: 人,小鼠
WB
¥600元
规格:
在线咨询
MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: WBSCR22 HUSSY-03 PP3381
  • 蛋白名称: WBS22
  • Human_gene_id: 114049
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=114049
  • Human_swiss_prot_no: O43709
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O43709/entry
  • Mouse_gene_id: 66138
  • Mouse_gene_link: https://www.uniprot.org/uniprot/66138
  • Mouse_swiss_prot_no: Q9CY21
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9CY21
  • 特异性: This antibody detects endogenous levels of WBS22 at Human/Mouse
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 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
  • 分子量: 31kD
  • 功能: disease:Haploinsufficiency of WBSCR22 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Methyltransferase that may act on DNA.,similarity:Belongs to the methyltransferase superfamily.,tissue specificity:Strongly expressed in heart, skeletal muscle and kidney. Also expressed in spleen, liver, lung and testis.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Nucleus, nucleoplasm . Cytoplasm, perinuclear region . Cytoplasm . Localized diffusely throughout the nucleus and the cytoplasm (PubMed:24488492). Localizes to a polarized perinuclear structure, overlapping partially with the Golgi and lysosomes (PubMed:25851604). Localization is not affected by glucocorticoid treatment (PubMed:24488492). .
  • 组织表达: Widely expressed, with high levels in heart, skeletal muscle and kidney. Detected at high levels in bronchial brushings and in normal lung (at protein level). In fetal lung tissue, expressed in the developing bronchial lumen lining cells (at protein level). Tends to be down-regulated in lungs affected by inflammatory diseases or neoplasia (at protein level). Expressed in immune cells, including B and T lymphocytes and macrophages.
  • 科研货号: PLA009243
WBS22 rabbit pAb
Catalog No PLA009243
Product information
  • 发货日期: 7
  • 基因名称: WBSCR22 HUSSY-03 PP3381
  • 蛋白名称: WBS22
  • Human_gene_id: 114049
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=114049
  • Human_swiss_prot_no: O43709
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O43709/entry
  • Mouse_gene_id: 66138
  • Mouse_gene_link: https://www.uniprot.org/uniprot/66138
  • Mouse_swiss_prot_no: Q9CY21
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9CY21
  • 特异性: This antibody detects endogenous levels of WBS22 at Human/Mouse
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 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
  • 分子量: 31kD
  • 功能: disease:Haploinsufficiency of WBSCR22 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Methyltransferase that may act on DNA.,similarity:Belongs to the methyltransferase superfamily.,tissue specificity:Strongly expressed in heart, skeletal muscle and kidney. Also expressed in spleen, liver, lung and testis.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Nucleus, nucleoplasm . Cytoplasm, perinuclear region . Cytoplasm . Localized diffusely throughout the nucleus and the cytoplasm (PubMed:24488492). Localizes to a polarized perinuclear structure, overlapping partially with the Golgi and lysosomes (PubMed:25851604). Localization is not affected by glucocorticoid treatment (PubMed:24488492). .
  • 组织表达: Widely expressed, with high levels in heart, skeletal muscle and kidney. Detected at high levels in bronchial brushings and in normal lung (at protein level). In fetal lung tissue, expressed in the developing bronchial lumen lining cells (at protein level). Tends to be down-regulated in lungs affected by inflammatory diseases or neoplasia (at protein level). Expressed in immune cells, including B and T lymphocytes and macrophages.
  • 科研货号: PLA009243
  • 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.
普拉特泽实验室电话助手

4006916686

扫码咨询