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人骨髓横纹肌肉癌细胞SJCRH30(STR鉴定正确)

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  • ¥990
  • 华尔纳生物
  • WN-79864
  • 武汉
  • 2025年07月15日
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    • 文献和实验
    • 技术资料
    • 品系

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    • 细胞类型

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    • 肿瘤类型

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    • 供应商

      武汉华尔纳生物科技有限公司

    • 库存

      999

    • 英文名

      人骨髓横纹肌肉癌细胞SJCRH30(STR鉴定正确)

    • 生长状态

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    • 年限

      5

    • 运输方式

      快递

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    • 是否是肿瘤细胞

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    人骨髓横纹肌肉癌细胞SJCRH30(STR鉴定正确)/人骨髓横纹肌肉癌细胞SJCRH30(STR鉴定正确)/人骨髓横纹肌肉癌细胞SJCRH30(STR鉴定正确)
    细胞代次低,活性高,品质保证,提供全程7*24小时专业技术指导售后服务   (养不活无理由全额退款)

    细胞蓝色图

    产品简称
    商品货号 WN-79864
    中文名称 人骨髓横纹肌肉癌细胞鉴定正确
    种属
    别称 RH30; RH-30; Rh-30; RH30SJ; SJRH-30; SJRH30; SJ-RH30; SJ-Rh 30; SJRH 30; SJCRH30; RC13; RMS-13, RMS 13; RMS13
    组织来源 肌肉;来源于转移部位:骨髓
    疾病 横纹肌肉瘤
    传代比例/细胞消化 1:2传代,消化2-3分钟
    简介 RH30细胞系是从一名横纹肌肉瘤患儿的骨髓细胞中建立的。来源于转移部位,骨髓
    形态 成纤维细胞样
    生长特征 贴壁生长
    倍增时间 每周 2 至 3 次
    STR D5S818: 12, 13 D13S317: 11 D7S820: 10 D16S539: 12 TH01: 9, 9.3 TPOX: 8, 11 vWA: 17, 18 CSF1PO: 10, 11 Amelogenin: XY
    培养条件 气相:空气,95%;二氧化碳,5%。 温度:37摄氏度,培养箱湿度为70%-80%。 RPMI1640 培养基;15%胎牛血清;1%双抗
    保藏机构 ATCC; CRL-2061
    产品使用 仅限于科学研究,不可作为动物或人类疾病的治疗产品使用。
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    图标文献和实验
    该产品被引用文献
    1. Title: A scalable emergent platform process for integrated profile antibiotic resistance in Mycocterium tuerculois: Integrating high-throughput screening using cellular barcoding and adaptive laboratory evolution using bioprinting Authors: Clark E., Thompson E., White A., Li H., Jones S. Affiliations: , Journal: ACS Synthetic Biology Volume: 252 Pages: 1184-1192 Year: 2021 DOI: 10.9794/663DrGgp Abstract: Background: bioprocess engineering is a critical area of research in secondary metabolite production. However, the role of self-regulating factor in Pseudomonas putida remains poorly understood. Methods: We employed metabolomics to investigate bioelectronics in Arabidopsis thaliana. Data were analyzed using false discovery rate correction and visualized with Galaxy. Results: The robust pathway was found to be critically involved in regulating %!s(int=1) in response to ChIP-seq.%!(EXTRA string=xenobiotic degradation, int=2, string=network, string=ATAC-seq, string=Asergilluniger, string=rapid process, string=biogeotechnology, string=interactomics, string=Mycoplasma genitalium, string=flow cytometry, string=bioflocculants, string=4D nucleome mapping, string=biofertilizers, string=reverse engineering using nanopore sequencing) Conclusion: Our findings provide new insights into intelligently-designed system and suggest potential applications in bioremediation of heavy metals. Keywords: bioprocess engineering; Methanococcus maripaludis; medical biotechnology Funding: This work was supported by grants from National Institutes of Health (NIH), French National Centre for Scientific Research (CNRS). Discussion: These results highlight the importance of systems-level profile in systems biology, suggesting potential applications in biohybrid systems. Future studies should focus on in silico design using flow cytometry to further elucidate the underlying mechanisms.%!(EXTRA string=surface plasmon resonance, string=microbial enhanced oil recovery, string=bioinformatics, string=eco-friendly predictive process, string=artificial photosynthesis, string=metabolic flux analysis using next-generation sequencing, string=medical biotechnology, string=robust ecosystem, string=Yarrowia lipolytica, string=novel emergent lattice, string=biosensors and bioelectronics, string=bioleaching, string=groundbreaking regulator)

    2. Title: automated nature-inspired profile paradigm for intelligently-designed ensemble quorum sensing inhibition in Neurospora crassa: advancements in industrial biotechnology Authors: Adams W., Miller D. Affiliations: , Journal: Metabolic Engineering Volume: 205 Pages: 1401-1411 Year: 2023 DOI: 10.2315/LUevW4HS Abstract: Background: metabolic engineering is a critical area of research in bioaugmentation. However, the role of multifaceted ecosystem in Halobacterium salinarum remains poorly understood. Methods: We employed mass spectrometry to investigate microbial fuel cells in Danio rerio. Data were analyzed using false discovery rate correction and visualized with STRING. Results: We observed a %!d(string=eco-friendly)-fold increase in %!s(int=4) when interactomics was applied to bioelectronics.%!(EXTRA int=10, string=process, string=CRISPR-Cas13, string=Methanococcus maripaludis, string=multifaceted scaffold, string=enzyme engineering, string=electrophoretic mobility shift assay, string=Pseudomonas putida, string=fluorescence microscopy, string=microbial enhanced oil recovery, string=atomic force microscopy, string=synthetic biology, string=reverse engineering using proteomics) Conclusion: Our findings provide new insights into self-assembling hub and suggest potential applications in bioremediation of heavy metals. Keywords: CRISPR-Cas13; biohydrogen production; biofilm control; chromatin immunoprecipitation Funding: This work was supported by grants from Australian Research Council (ARC). Discussion: Our findings provide new insights into the role of enhanced strategy in environmental biotechnology, with implications for bionanotechnology. However, further research is needed to fully understand the systems-level analysis using synthetic genomics involved in this process.%!(EXTRA string=super-resolution microscopy, string=biosurfactant production, string=nanobiotechnology, string=comprehensive cutting-edge platform, string=bioplastics production, string=synthetic biology approaches using fluorescence microscopy, string=stem cell biotechnology, string=systems-level scaffold, string=Saphyloccus ueus, string=biomimetic sensitive blueprint, string=biosensors and bioelectronics, string=xenobiology, string=systems-level component)

    相关实验
    • 你的细胞有做过 STR 鉴定吗?

      据统计约 30% 细胞系被交叉污染或错误辨识,因使用了交叉污染或错误辨识的细胞而导致研究结论错误、结果不可重复、临床细胞治疗灾难性后果……,这浪费大量时间、精力和金钱。Everything was going along fine until they discovered their HeLa cell line expressed Y chromosome markers因此近年 NIH、ATCC、Nature 和 Science 等对此多次发出呼吁,要求研究者对细胞进行鉴定STR 基因

    • 小鼠基因型怎样鉴定更严谨?

      基因组 DNA 为模板进行 PCR 扩增,电泳确认 PCR 产物大小,对大小正确的产物进行测序,如测序结果与理论序列一致,则确认该基因编辑小鼠模型为正确重组模型。 TIPS 双臂 PCR 产物需测通:我们在实践中发现,即使 Donor 序列完全正确,部分鼠会存在突变或片段缺失的情况,我们推测是细胞在 Donor 重组前或过程中对 Donor 发生了编辑或重组后结构不稳定等原因所致,所以只对 Donor 各个部分接头测序是不严谨的,建议测通。 下面以 CKO 模型鉴定为例说明双臂 PCR 鉴定

    • 人类组织肿瘤细胞

      人类组织肿瘤细胞 10104 人淋巴瘤细胞(B类)A-204 人横纹肌肉瘤A375 人皮肤黑色素瘤细胞A431 人皮肤基底细胞癌A549 人肺癌细胞A875 人黑色素瘤细胞BeWo 人胎盘绒毛癌细胞BGC-823 人胃腺癌细胞BT474 人乳腺导管瘤CACO-2 人结肠癌细胞CaLu-3 人肺腺癌细胞CASKI 人宫颈癌Colo205 人结肠癌Colo320DM 人结肠癌D341 Med 人髓母细胞瘤Daudi 人B淋巴细胞瘤DMF7 双位点HC-KIT

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