UltraScence Pico/Femto Ultra Western Substrate

UltraScence Pico/Femto Ultra Western Substrate

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UltraScence Pico/Femto Ultra Western Substrate

*Mix and Match excluded from promo

Starting at $40.00

Size:
Grouped product items
Wishlist Product Name Cat# Size Qty
UltraScence Pico Ultra Western Substrate
Special Price $40.00 $79.00
CCH345-B100ML 50ml x 2/Set
UltraScence Femto Western Substrate
Special Price $50.00 $399.00
CCH365-B100ML 50ml x 2/Set

Description

The UltraScence Pico Ultra Western Substrate, as a luminol-based enhanced chemiluminescent substrate, is sensitive and compatible with conducting immunoblots with horseradish peroxidase (HRP) – conjugated secondary antibodies. The low picogram to mid femtogram detection of antigen is enabled by UltraScence Pico Ultra Western Substrate’s excellent sensitivity and long signal duration. Further, its long chemiluminescent signal duration makes both digital and film-based imaging possible without any loss of the signal. Appropriate primary and secondary antibody dilutions are suggested for attaining optimal signal intensity and duration.

The UltraScence Femto Western Substrate, as a luminol-based enhanced chemiluminescent substrate, is sensitive and compatible with conducting immunoblots with horseradish peroxidase (HRP) conjugated secondary antibodies. The mid femtogram to low femtogram detection of antigen is enabled by UltraScence Femto Western Substrate excellent sensitivity and long signal duration. Further, its long chemiluminescent signal duration makes both digital and film-based imaging possible without any loss of the signal. Appropriate primary and secondary antibody dilutions are suggested for attaining optimal signal intensity and duration.

Citations

  1. Suryavanshi, S. V., Zaiachuk, M., Pryimak, N., Kovalchuk, I., & Kovalchuk, O. (2022). Cannabinoids Alleviate the LPS-Induced Cytokine Storm via Attenuating NLRP3 Inflammasome Signaling and TYK2-Mediated STAT3 Signaling Pathways In Vitro. Cells11(9), 1391.

    Article | CCH345-B100ML

  2. Grozavu, I., Stuart, S., Lyakisheva, A., Yao, Z., Pathmanathan, S., Ohh, M., & Stagljar, I. (2022). D154Q mutation does not alter KRAS dimerization. Journal of Molecular Biology434(2), 167392.

    Article | CCH345-B100ML

  3. Burnie, J., Persaud, A. T., Thaya, L., Liu, Q., Miao, H., Grabinsky, S., ... & Guzzo, C. (2022). P-selectin glycoprotein ligand-1 (PSGL-1/CD162) is incorporated into clinical HIV-1 isolates and can mediate virus capture and subsequent transfer to permissive cells. Retrovirology19(1), 1-22.

    Article | SL100688 | CCH365-B100ML

  4. Lyons, B. J., Atkinson, C. E., Deng, W., Serapio-Palacios, A., Finlay, B. B., & Strynadka, N. C. (2021). Cryo-EM structure of the EspA filament from enteropathogenic Escherichia coli: revealing the mechanism of effector translocation in the T3SS. Structure29(5), 479-487.

    Article | CCH345-B100ML

  5. Misner, M. J., Taborek, A., Dufour, J., Sharifi, L., Khokhar, J. Y., & Favetta, L. A. (2021). Effects of Delta-9 Tetrahydrocannabinol (THC) on Oocyte Competence and Early Embryonic Development. Frontiers in Toxicology, 14.

    Article | CCH345-B100ML

  6. Lee, Y. C., Dean, G. H., Gilchrist, E., Tsai, A. Y. L., & Haughn, G. W. (2021). Asymmetric distribution of extracellular matrix proteins in seed coat epidermal cells of Arabidopsis is determined by polar secretion. Plant direct5(11), e360.

    Article | CCH365-B100ML

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