公司产品仅供科研研究实验，不得用于临床！
商品详情：
英文名称：SLAIN1
中文名称：13号染色体开放阅读框32抗体
别 名；C13orf32; chromosome 13 open reading frame 32; FLJ30046; MGC131899; SLAI1_HUMAN; SLAIN motif family member 1; SLAIN motif family, member 1; SLAIN motif-containing protein 1; Slain1.
研究领域；肿瘤 细胞生物 神经生物学 干细胞
抗体来源；Rabbit
克隆类型；Polyclonal
交叉反应；(predicted: Human, Mouse, Rat, Chicken, Dog, Rabbit, )
产品应用；ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量；61kDa
细胞定位；细胞浆
性 状；Liquid
浓 度；1mg/ml
免 疫 原；KLH conjugated synthetic peptide derived from human SLAIN1/C13orf32: 1-100/568
亚 型；IgG
纯化方法；affinity purified by Protein A
缓 冲 液；0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件；Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项；This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍；SLAIN1 is a 561 amino acid member of the SLAIN motif-containing family and is expressed in embryonic stem cells, as well as in lung, brain and testis, where it exists as two alternatively spliced isoforms. The gene encoding SLAIN1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
Tissue Specificity:
Expressed in embryonic stem cells.
扫描二维码
扫描二维码
资料/datasheet
