超敏ECL发光底物检测试剂盒(飞克级)
货号:PMK0448
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价格:
400.00
规格:
100ml
500ml
货期:
现货
本产品4 ℃运输,保存于4℃,保质期 12个月。
Details
产品详情
  • 产品简介

    普美克生产的超敏ECL发光底物检测试剂盒用于检测直接或间接标记辣根过氧化物酶(HRP)的抗体及其关联的抗原。其原理是,蛋白质或核酸在电泳后转移到印迹膜上,以一抗及HRP标记的二抗结合膜上的目的蛋白,或以HRP标记的探针直接或间接结合膜上的核酸。洗膜后用本产品配制的ECL工作液,室温孵育膜数分钟,将印迹膜用保鲜膜包被粘贴固定于X光片曝光暗盒。然后转入暗室将X光胶片压在膜上曝光数秒到数小时,显影定影后蛋白质或核酸条带可清晰显示在X光胶片上。

    本产品采用独特的发光底物系统,降低曝光背景的同时引入新型的氧化剂,大大提高试剂盒的稳定性,使其在室温能稳定放置一年。本产品配制的ECL工作液衰减较慢,15min内荧光几无减弱,检测时产生的非特异背景非常低,也可节省抗体和待测样品的用量,该试剂可用于PVDF膜和NC膜(硝酸纤维素膜)的Western blot免疫印迹等印迹发光显色。除用于X光胶片,还可直接使用荧光CCD扫描。

  • 注意事项

    1、为了您的安全和健康,请穿实验服并戴一次性手套操作。

    2、本产品A液和B液均对人体有害,操作时请小心,并注意有效防护避免直接接触人体或吸入体内。本产品仅限于专业人员的科学研究用,不得用于临床诊断或治疗,不得用于食品或药品,不得存放于普通住宅内。

Instruction manual/COA download
说明书/COA下载
Published literature
已发表文献
  • 1.Liu H ,Liu Z ,Liang W , et al.Tea leaf-derived nanovesicles for ferric-supply-amplified ICD and macrophage reprogramming to boost immunotherapy against head and neck squamous carcinoma[J].Chemical Engineering Journal,2025,503158469-158469. (IF 13.3)

    2. Peiyu L ,Xinyi Z ,Yahui Z , et al.Neurotoxic A1 astrocytes promote neuronal ferroptosis via CXCL10/CXCR3 axis in epilepsy.[J].Free radical biology & medicine,2023,195. (IF 7.4)

    3. Xinyi Z ,Peiyu L ,Yahui Z , et al.Blockade of Kv1.3 Potassium Channel Inhibits Microglia-Mediated Neuroinflammation in Epilepsy[J].International Journal of Molecular Sciences,2022,23(23):14693-14693. (IF 6.208)

    4. Yerlan B ,Wenqi L ,Muguli M , et al.Ferula ferulaeoides ethyl acetate extract induces apoptosis in esophageal cancer cells via mitochondrial and PI3K/Akt/Bad pathways[J].Arabian Journal of Chemistry,2023,16(12): (IF 6)

    5. Peng B ,Wang L ,Pan S , et al.Metformin Attenuates Partial Epithelial-Mesenchymal Transition in Salivary Gland Inflammation via PI3K/Akt/GSK3β/Snail Signaling Axis[J].Inflammation,2024,(prepublish):1-13. (IF 4.5)

    6.Liu W ,Deng J ,Tao J X , et al.Aurantioobtusin regulates lipogenesis and ferroptosis of liver cancer cells through inhibiting SCD1 and sensitizing RSL3.[J].International journal of oncology,2024,65(4):  (IF 4.5)

    7.Zhoujia H ,Wei Z ,Lin H , et al.Kaempferol exerts antioxidant effects in age-related diminished ovarian reserve by regulating the HSP90/NRF2 pathway.[J].Chemical biology & drug design,2023,103(1):  (IF 3 )

    8.Wang D ,Wang J ,Yao F , et al.miR-1247-3p regulation of CCND1 affects chemoresistance in colorectal cancer.[J].PloS one,2024,19(12):e0309979. (IF 2.9)

    9.Wen H ,Yuan L ,Wei C , et al.Effects of combined exposure to formaldehyde and benzene on immune cells in the blood and spleen in Balb/c mice[J].Environmental Toxicology and Pharmacology,2016,45265-273. (IF 2.187)

    10. Wei Q ,ChengShi X ,XiaoChong L , et al. Telmisartan inhibits microglia-induced neurotoxic A1 astrocyte conversion via PPARγ-mediated NF-κB/p65 degradation.[J].International immunopharmacology,2023,123110761-110761. (IF 5.6)

    11. Chenxi W ,Huaxiao W ,Langyue Y , et al.Formaldehyde induces toxicity in mouse bone marrow and hematopoietic stem/progenitor cells and enhances benzene-induced adverse effects.[J].Archives of toxicology,2017,91(2):921-933. (IF 6.637)

    12. Liu S ,Wang Y ,Ying L , et al.Quercetin Mitigates Lysophosphatidylcholine (LPC)-Induced Neutrophil Extracellular Traps (NETs) Formation through Inhibiting the P2X7R/P38MAPK/NOX2 Pathway[J].International Journal of Molecular Sciences,2024,25(17):9411-9411. (IF 4.9)

    13. Li G ,Wu M ,Chen K , et al.ROS-mediated M1 polarization-necroptosis crosstalk involved in Di-(2-ethylhexyl) phthalate-induced chicken liver injury.[J].Poultry science,2024,104(1):104558. (IF 3.8)

    14. Yuan Z L ,Tian L ,Feng T , et al.ZDHHC15 promotes glioma malignancy and acts as a novel prognostic biomarker for patients with glioma[J].BMC Cancer,2023,23(1):420-420. (IF 3.8)

    15. Wei C ,Chen M ,You H , et al.Formaldehyde and co-exposure with benzene induce compensation of bone marrow and hematopoietic stem/progenitor cells in BALB/c mice during post-exposure period[J].Toxicology and Applied Pharmacology,2017,32436-44. (IF 3.791)

Product Q&A FAQ
产品问答FAQ
  • Western Blot(WB)实验中有很多杂带咋回事?

    答:可能的原因有:

    1、目的蛋白有多个修饰位点,本身可以呈现多条带,建议查阅文献或进行生物信息学分析,获得蛋白序列的修饰位点信息,通过去修饰确定蛋白实际大小;

    2、样本处理过程中目的蛋白发生降解,建议加入蛋白酶抑制剂;样本处理时在冰上操作;

    3、杂蛋白多,建议处理目的蛋白;

    4、抗体特异性不强,建议使用特异性强的抗体;

    5、抗体孵育时间过久,建议减少抗体孵育时间;

    6、二抗与抗原有交叉反应,建议选择合适的封闭物;

    7、二聚体或多聚体存在,建议增加蛋白质变性过程及强度;

    8、底物显色与曝光时间过长,建议缩短显色及曝光的时间。


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