Block ACE
Block Ace blocking reagent (BUF029A) used to supress non-specific binding in a sandwich ELISA for the evaluation of anti-tau antibodies.
Image caption:
Novel tau mAbs selectively bind AD-tau compared to tau monomer. a Sandwich ELISA assay comprised of total tau capture antibody K9JA and three distinct tau antigens, AD-tau, AD-P1 PFFs, and tau monomer, detected by novel tau mAbs DMR7 or SKT82 and total tau antibody Tau5 as a loading control demonstrating similar levels of captured antigen for each form of tau.
From: Gibbons GS, Kim SJ, Wu Q, Riddle DM, Leight SN, Changolkar L, Xu H, Meymand ES, O'Reilly M, Zhang B, Brunden KR, Trojanowski JQ, Lee VMY.
Conformation-selective tau monoclonal antibodies inhibit tau pathology in primary neurons and a mouse model of Alzheimer's disease.
Mol Neurodegener. 2020 Nov 4;15(1):64
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
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.
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.
Product Details
- Reconstitution
- Reconstitute each 4g sachet in 100ml distilled water.
Storage Information
- Storage
- Store at +4oC. DO NOT FREEZE.
This product should be stored undiluted. Should this product contain a precipitate we recommend microcentrifugation before use. - 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.
More Information
- Regulatory
- For research purposes only
Applications of Block ACE
| 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
Copyright © 2021 Bio-Rad Antibodies (formerly AbD Serotec)
Product Specific References
References for Block ACE
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Yamashita, M. et al. (2010) Morphological and extracellular matrix changes following vocal fold injury in mice.
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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. -
Hara, H. et al. (1990) Enzyme immunoassay for measuring antibodies against skeletal muscle in patients with myasthenia gravis.
Clin Chem. 36 (11): 1967-9. -
Shinmoto, H. et al. (1988) Production of pentameric hybrid immunoglobulins consisting of IgA and IgM.
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Ahmed, R.R. et al. (2010) BACE1 and BACE2 enzymatic activities in Alzheimer's disease.
J Neurochem. 112: 1045-53. -
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. -
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. -
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. -
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. -
Yamashita, M. et al. (2009) Surgical method to create vocal fold injuries in mice.
Ann Otol Rhinol Laryngol. 118: 131-8. -
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. -
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. -
Tarhan, Y.E. et al. (2016) Morphological Changes, Cadherin Switching, and Growth Suppression in Pancreatic Cancer by GALNT6 Knockdown
Neoplasia 18: 265-72. -
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. -
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. -
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. -
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. -
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. -
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. -
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. -
Ling, C. et al. (2019) Differentiated fibrocytes assume a functional mesenchymal phenotype with regenerative potential.
Sci Adv. 5 (5): eaav7384.
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