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Block ACE

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BUF029
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Block Ace is designed as a high-performance blocking reagent for use in immunological assays such as ELISA and Western blotting. It may also be used for dilution of antibodies and for washing procedures in the above assays.

Block Ace has been shown to have superior performance to 1% BSA in blocking in ELISA assays. In comparison to BSA, Block Ace provides reduced backgrounds and sharper standard curves.

For blocking in ELISA applications, we recommend using a 1/4 dilution of the reconstituted solution.

For blocking in Western Blotting applications, we recommend using the reconstituted solution neat.

For washing applications we recommend a 1/10 dilution of the reconstituted solution, and adding Tween 20 to a level of 0.05-0.2% v/v.

For use as a test sample or secondary antibody diluent we recommend a 1/10 dilution of the reconstituted solution.

Reconstitution
Reconstitute each 4g sachet in 100ml distilled water.
Regulatory
For research purposes only
Guarantee
Guaranteed for 1 week from the date of reconstitution or until the date of expiry, whichever comes first. Please see label for expiry date.

Store at +4oC. DO NOT FREEZE.
This product should be stored undiluted. Should this product contain a precipitate we recommend microcentrifugation before use.

This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit the antibody protocols page.
Application Name Verified Min Dilution Max Dilution
ELISA 1/4
Western Blotting Neat
Where this product has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the reagent for use in their own system using appropriate negative/positive controls

References for Block ACE

  1. Shinmoto, H. et al. (1988) Production of pentameric hybrid immunoglobulins consisting of IgA and IgM.
    Agric. Biol. Chem. 52:2653-2654.
  2. Hara, H. et al. (1990) Enzyme immunoassay for measuring antibodies against skeletal muscle in patients with myasthenia gravis.
    Clin Chem. 36 (11): 1967-9.
  3. Yamashita, M. et al. (2009) Surgical method to create vocal fold injuries in mice.
    Ann Otol Rhinol Laryngol. 118: 131-8.
  4. Yamashita, M. et al. (2010) Morphological and extracellular matrix changes following vocal fold injury in mice.
    Cells Tissues Organs. 192 (4): 262-71.
  5. Head, E. et al. (2010) Amyloid-beta peptide and oligomers in the brain and cerebrospinal fluid of aged canines.
    J Alzheimers Dis. 2010;20(2):637-46.
  6. Ahmed, R.R. et al. (2010) BACE1 and BACE2 enzymatic activities in Alzheimer's disease.
    J Neurochem. 112: 1045-53.
  7. Matsui, T.S. et al. (2011) Non-muscle myosin II induces disassembly of actin stress fibres independently of myosin light chain dephosphorylation.
    Interface Focus. 1 (5): 754-66.
  8. Zhang, B. et al. (2012) The microtubule-stabilizing agent, epothilone D, reduces axonal dysfunction, neurotoxicity, cognitive deficits, and Alzheimer-like pathology in an interventional study with aged tau transgenic mice.
    J Neurosci. 32 (11): 3601-11.
  9. View The Latest Product References
  10. Fitz, N.F. et al. (2012) Abca1 Deficiency Affects Alzheimer's Disease-Like Phenotype in Human ApoE4 But Not in ApoE3-Targeted Replacement Mice.
    J Neurosci. 32: 13125-36.
  11. Habara, P. et al. (2012) Novel flow cytometric method for the detection of podocalyxin-positive elements in urine of patients with glomerulonephritides - first promising results.
    Folia Biol (Praha). 58: 57-63.
  12. Qosa, H. et al. (2015) Extra-virgin olive oil attenuates amyloid-β and tau pathologies in the brains of TgSwDI mice.
    J Nutr Biochem. 26 (12): 1479-90.
  13. Faraj SF et al. (2015) Assessment of tumoral PD-L1 expression and intratumoral CD8+ T cells in urothelial carcinoma.
    Urology. 85 (3): 703.e1-6.
  14. Wilcock DM et al. (2015) Down syndrome individuals with Alzheimer's disease have a distinct neuroinflammatory phenotype compared to sporadic Alzheimer's disease.
    Neurobiol Aging. 36 (9): 2468-74.
  15. Kim, J.A. et al. (2015) Magnetic bead droplet immunoassay of oligomer amyloid β for the diagnosis of Alzheimer's disease using micro-pillars to enhance the stability of the oil-water interface.
    Biosens Bioelectron. 67: 724-32.
  16. Wilcock, D.M. et al. (2015) Down syndrome individuals with Alzheimer's disease have a distinct neuroinflammatory phenotype compared to sporadic Alzheimer's disease.
    Neurobiol Aging. 36 (9): 2468-74.
  17. Hashitani, H. et al. (2015) Pacemaker role of pericytes in generating synchronized spontaneous Ca2+ transients in the myenteric microvasculature of the guinea-pig gastric antrum.
    Cell Calcium. 58 (5): 442-56.
  18. Tarhan, Y.E. et al. (2016) Morphological Changes, Cadherin Switching, and Growth Suppression in Pancreatic Cancer by GALNT6 Knockdown.
    Neoplasia. 18 (5): 265-72.
  19. Park, M.C. et al. (2016) Droplet-based magnetic bead immunoassay using microchannel-connected multiwell plates (μCHAMPs) for the detection of amyloid beta oligomers.
    Lab Chip. 16 (12): 2245-53.
  20. Kanzaki, H. et al. (2017) Phosphoglycerol dihydroceramide, a distinctive ceramide produced by Porphyromonas gingivalis, promotes RANKL-induced osteoclastogenesis by acting on non-muscle myosin II-A (Myh9), an osteoclast cell fusion regulatory factor.
    Biochim Biophys Acta. 1862 (5): 452-462.
  21. Ling, C. et al. (2019) Differentiated fibrocytes assume a functional mesenchymal phenotype with regenerative potential.
    Sci Adv. 5 (5): eaav7384.
  22. Gibbons, G.S. et al. (2020) Conformation-selective tau monoclonal antibodies inhibit tau pathology in primary neurons and a mouse model of Alzheimer's disease.
    Mol Neurodegener. 15 (1): 64.
  23. Marotta, N.P. et al. (2021) Alpha-synuclein from patient Lewy bodies exhibits distinct pathological activity that can be propagated in vitro.
    Acta Neuropathol Commun. 9 (1): 188.
  24. Uemura, N. et al. (2023) α-Synuclein aggregates amplified from patient-derived Lewy bodies recapitulate Lewy body diseases in mice.
    Nat Commun. 14 (1): 6892.
  25. Bassil, F. et al. (2020) Amyloid-Beta (Aβ) Plaques Promote Seeding and Spreading of Alpha-Synuclein and Tau in a Mouse Model of Lewy Body Disorders with Aβ Pathology
    Neuron. 105 (2): 260-275.e6.
  26. Chakrabarty, P. et al. (2018) TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease.
    J Exp Med. 215 (9): 2247-64.
  27. Yang, Y. et al. (2018) Plasma Oligomeric Beta Amyloid in Alzheimer's Disease with History of Agent Orange Exposure.
    Dement Neurocogn Disord. 17 (2): 41-9.
  28. Lubben, N. et al. (2024) LRRK2 kinase inhibition reverses G2019S mutation-dependent effects on tau pathology progression.
    Transl Neurodegener. 13 (1): 13.

Immunofluorescence

Western Blotting

BUF029

148689 151662 156616 159197 161050 165345 165662 165728

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