获取电话英文名称 RSL1D1
中文名称 细胞衰老抑制基因蛋白抗体
别 名 CATX 11; CATX-11; CATX11; Cellular senescence inhibited gene protein; Cellular senescence-inhibited gene protein; CSIG; L12; PBK1; Protein PBK1; Ribosomal L1 domain containing 1; Ribosomal L1 domain-containing protein 1; RL1D1_HUMAN; RSL1D1.
细胞衰老抑制基因蛋白抗体
说 明 书 0.2ml
研究领域 肿瘤 细胞生物 信号转导 细胞周期蛋白 细胞分化 表观遗传学
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Cow, Sheep,
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 55kDa
细胞定位 细胞核
性 状 Lyophilized or Liquid
浓 度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human RSL1D1
亚 型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
细胞衰老抑制基因蛋白抗体产品介绍 background:
RSL1D1, also known as CATX-11, PBK1, L12 or CSIG, is a 490 amino acid nuclear protein that belongs to the ribosomal protein L1P family. Expressed in placenta, RSL1D1 contains many phosphorylated amino acid residues and is encoded by a gene that maps to human chromosome 16p13.13. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias.
Subcellular Location:
Nucleus
Tissue Specificity:
Placenta
Similarity:
Belongs to the ribosomal protein L1P family. Highly divergent.
Gene ID:
26156
Database links:
Entrez Gene: 26156 Human
SwissProt: O76021 Human
Unigene: 401842 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
细胞衰老抑制基因蛋白抗体
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