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MRP-S16 Polyclonal Antibody
商品货号: PLA016912
适 应 性: 人,小鼠
WB IHC IF ELISA
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: MRPS16
  • 蛋白名称: 28S ribosomal protein S16 mitochondrial
  • Human_gene_id: 51021
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51021
  • Human_swiss_prot_no: Q9Y3D3
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q9Y3D3/entry
  • Mouse_gene_id: 66242
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=66242
  • Mouse_swiss_prot_no: Q9CPX7
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q9CPX7
  • 特异性: MRP-S16 Polyclonal Antibody detects endogenous levels of MRP-S16 protein.
  • 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 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
  • 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
  • 其他名称: MRPS16; RPMS16; CGI-132; 28S ribosomal protein S16; mitochondrial; MRP-S16; S16mt
  • 实测条带: 15kD
  • 功能: disease:Defects in MRPS16 are the cause of combined oxidative phosphorylation deficiency type 2 (COXPD2) [MIM:610498]. Defects in the mitochondrial oxidative phosphorylation system result in devastating, mainly multisystem, diseases. COXPD2 symptoms include fatal neonatal metabolic acidosis with agenesis of the corpus callosum.,similarity:Belongs to the ribosomal protein S16P family.,subunit:Component of the mitochondrial ribosome small subunit (28S) which comprises a 12S rRNA and about 30 distinct proteins.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Mitochondrion .
  • 组织表达: Muscle,
  • 科研货号: PLA016912
MRP-S16 Polyclonal Antibody
Catalog No PLA016912
Product information
  • 基因名称: MRPS16
  • 蛋白名称: 28S ribosomal protein S16 mitochondrial
  • Human_gene_id: 51021
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51021
  • Human_swiss_prot_no: Q9Y3D3
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q9Y3D3/entry
  • Mouse_gene_id: 66242
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=66242
  • Mouse_swiss_prot_no: Q9CPX7
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q9CPX7
  • 特异性: MRP-S16 Polyclonal Antibody detects endogenous levels of MRP-S16 protein.
  • 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 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
  • 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
  • 其他名称: MRPS16; RPMS16; CGI-132; 28S ribosomal protein S16; mitochondrial; MRP-S16; S16mt
  • 实测条带: 15kD
  • 功能: disease:Defects in MRPS16 are the cause of combined oxidative phosphorylation deficiency type 2 (COXPD2) [MIM:610498]. Defects in the mitochondrial oxidative phosphorylation system result in devastating, mainly multisystem, diseases. COXPD2 symptoms include fatal neonatal metabolic acidosis with agenesis of the corpus callosum.,similarity:Belongs to the ribosomal protein S16P family.,subunit:Component of the mitochondrial ribosome small subunit (28S) which comprises a 12S rRNA and about 30 distinct proteins.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Mitochondrion .
  • 组织表达: Muscle,
  • 科研货号: PLA016912
  • 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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