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    products/chip-kits/beta-secretase-activity-assay-kit-fluorometric-ab65357.pdf

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Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)

  • Datasheet
  • SDS
  • Protocol Booklet
Reviews (1)Q&A (16)References (31)

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Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)

Key features and details

  • Assay type: Enzyme activity
  • Detection method: Fluorescent
  • Platform: Microplate reader
  • Assay time: 1 hr
  • Sample type: Cell culture media, Cell Lysate, Other biological fluids, Plasma, Serum, Tissue Lysate, Urine

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Overview

  • Product name

    Beta Secretase Activity Assay Kit (Fluorometric)
    See all Beta secretase kits
  • Detection method

    Fluorescent
  • Sample type

    Urine, Serum, Plasma, Other biological fluids, Cell Lysate, Cell culture media, Tissue Lysate
  • Assay type

    Enzyme activity
  • Assay time

    1h 00m
  • Species reactivity

    Reacts with: Mammals, Other species
  • Product overview

    Beta Secretase Activity Assay Kit (ab65357) uses a convenient fluorescence method for detecting beta secretase activity in biological and purified samples.


    The beta secretase assay protocol uses a secretase-specific peptide conjugated to two reporter molecules, EDANS and DABCYL. In the uncleaved form, the fluorescent signal from EDANS is quenched by the physical proximity of the DABCYL moiety. Cleavage of the peptide by beta secretase physically separates EDANS and DABCYL allowing for the release of a fluorescent signal. The level of secretase enzymatic activity in samples is proportional to the level of fluorescence intensity.

  • Notes

    This product is manufactured by BioVision, an Abcam company and was previously called K360 Beta-Secretase Activity Fluorometric Assay Kit. K360-100 is the same size as the 100 test size of ab65357.

    β-Secretase (Beta secretase) is responsible for the proteolytic process of the amyloid precursor protein (APP). It cleaves APP at the N-terminus of the A-beta peptide sequence, between residues 671 – 672, leading to the generation and extracellular release of beta-cleaved soluble APP, and a corresponding cell-associated C-terminal fragment which is later released by gamma-secretase. It has been implicated to be an excellent target for anti-amyloid therapy for the treatment of Alzheimer’s disease.

    The standard is affinity purified.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -80°C. Please refer to protocols.
  • Components Identifier 100 tests
    β -Secretase Extraction Buffer NM 1 x 25ml
    β -Secretase Inhibitor (in DMSO) Blue 1 x 10µl
    β -Secretase Reaction Buffer (2X) WM 1 x 10ml
    Active β -Secretase Red 1 x 20µl
    β -Secretase Substrate (in DMSO) Amber NM 1 x 200µl
  • Research areas

    • Neuroscience
    • Neurology process
    • Neurodegenerative disease
    • Alzheimer's disease
    • Proteases
    • Cell Biology
    • Proteolysis / Ubiquitin
    • Proteolytic enzymes
    • Aspartic protease
    • BACEs
    • Kits/ Lysates/ Other
    • Kits
    • Cell Metabolism Kits
    • Other Metabolism Assay
    • Kits/ Lysates/ Other
    • Kits
    • Cell Signaling Kits
    • Other Cell Signaling Kits
  • Relevance

    Beta secretase is a protease responsible for the proteolytic processing of the amyloid precursor protein (APP). Amyloid beta peptide is the major constituent of amyloid plaques in the brains of individuals afflicted with Alzheimers disease. This peptide is generated from the beta-amyloid precursor protein (beta APP) in a two-step process. The first step involves cleavage of the extracellular, amino-terminal domain of beta APP. Protein cleavage is performed by an aspartyl protease termed beta-secretase (BACE), of which there are two isoforms, BACE1 and 2. Beta APP cleavage by beta-secretase results in the cellular secretion of a segment of beta APP and a membrane-bound remnant. This remnant is then processed by another protease termed gamma-secretase. Gamma-secretase cleaves an intra-membrane site in the carboxyl-terminal domain of beta APP, thus generating the amyloid beta peptide.
  • Cellular localization

    Membrane; Single-pass type I membrane protein.
  • Alternative names

    • APP beta secretase
    • ASP 2
    • ASP2
    • BACE
    • BACE1
    • Beta secretase 1
    • Beta site APP cleaving enzyme 1
    • Memapsin2
    see all

Associated products

  • Related Products

    • Beta Secretase Substrate (ab101160)
    • Recombinant human BACE1 protein (Active) (ab168075)

Images

  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
    Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)

    Beta Secretase Activity measured in biological fluids. Tested neat. 

  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
    Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)

    Beta Secretase Activity measured in tissue lysates (each with protein concentration of 4 mg/mL)

  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
    Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)

    Beta Secretase Activity measured in cell lysates (each with concentration of 2e7 cells/mL).

  • Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
    Functional Studies - Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)
    Beta-Secretase Cleavage Activity assayed using ab65357.

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (31)

Publishing research using ab65357? Please let us know so that we can cite the reference in this datasheet.

ab65357 has been referenced in 31 publications.

  • Wang NY  et al. Ferulic Acid Ameliorates Alzheimer's Disease-like Pathology and Repairs Cognitive Decline by Preventing Capillary Hypofunction in APP/PS1 Mice. Neurotherapeutics 18:1064-1080 (2021). PubMed: 33786807
  • Baranowski BJ  et al. Examination of BDNF Treatment on BACE1 Activity and Acute Exercise on Brain BDNF Signaling. Front Cell Neurosci 15:665867 (2021). PubMed: 34017238
  • Sil S  et al. Astrocytes & Astrocyte derived Extracellular Vesicles in Morphine Induced Amyloidopathy: Implications for Cognitive Deficits in Opiate Abusers. Aging Dis 12:1389-1408 (2021). PubMed: 34527417
  • Sil S  et al. HIV-1 Tat-mediated astrocytic amyloidosis involves the HIF-1a/lncRNA BACE1-AS axis. PLoS Biol 18:e3000660 (2020). PubMed: 32453744
  • Michelon C  et al. The Role of Secretase Pathway in Long-term Brain Inflammation and Cognitive Impairment in an Animal Model of Severe Sepsis. Mol Neurobiol 57:1159-1169 (2020). PubMed: 31701437
View all Publications for this product

Customer reviews and Q&As

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1-10 of 17 Abreviews or Q&A

Beta-secretase activity in the mouse brain

Good Good 4/5 (Ease of Use)
Abreviews
Abreviews
abreview image
β-secretase activity in the mouse brain were measured using this kit. Solubilized membranes were extracted from brain tissues using β-secretase extraction buffer in this kit.
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Ms. Ji Hye Han

Verified customer

Submitted Jun 27 2018

Question



What extraction buffer are you suggesting to prepare tissue extracts (in my case it is mouse brain extracts)?

Can you reveal me composition of extraction buffer provided in the kit? It has protease inhibitors?

Read More

Abcam community

Verified customer

Asked on Jan 23 2015

Answer



We recommend to use 2 – 3x volume of ice-cold extraction buffer (provided with the kit) for tissue samples and to homogenize it on ice. The composition of the extraction buffer is proprietary information but I am happy to confirm that it contains DTT, Glycerol, EDTA, & NaAc.

As Beta secretase itself is a protease, there are no proteinase inhibitors added in this kit to make sure the target enzyme itself is not inhibited.

Read More

Anja Hoffmann

Abcam Scientific Support

Answered on Jan 23 2015

Question

Hello,

The kit (ab65357) works for biological samples. Can it be used to screen inhibitors dissolved in DMSO? Please let me know.

Read More

Abcam community

Verified customer

Asked on Dec 23 2014

Answer


I contacted the laboratories. This kit has not been tested with DMSO dissolved samples. However, I am sorry it is most likely that samples in DMSO will not work well since enzymes are sensitive to DMSO. Typically >1-2% DMSO is not recommended for any activity assay or for any cell treatment. DMSO can be toxic to cells.
Successfully tested species and applications covered by the guarantee are listed on our datasheets, and this is updated as soon as we have any further information. In this case, the kit has been tested in Urine, Serum, Plasma, Tissue Extracts, Cell Lysate, Cell culture media.

Read More

Sam Washer

Abcam Scientific Support

Answered on Dec 23 2014

Question

As I was trying other ways to measure beta-secretase activity before I ordered this kit, I already have frozen cell sample in 20 mM Sodium Citrate, pH 4.8 and 0.06% (v/v) Triton X-100.

I know you cannot tell me the formulation of the extraction buffer you use in this kit, but will the extraction buffer I have used (listed above) be compatible with the assay?

The cell samples were prepared in the following way:

1. Started with a confluent 35 mm dish of CHO cells

2. Removed media, washed cells 2x with 1xPBS, and collected cells in 100 uL of the solution listed above.

3. Stored samples at -80C.

If I started the ab65357 assay procedure from step 4a would you expect it be successful? I am assuming that the extraction buffer formulation is very similar to what I used.

A few additional questions:

1. If I were to harvest cells with the extraction buffer provided in the kit, can I store the samples at -80C before I perform the assay?

2. On page 7 of the assay protocol, it states that 5x10^6 cells/assay is needed. Is that correct? That means I have to use confluent 100 mm dishes for all my cell treatments. This doesn’t seem very practical and feels like a waste of reagents/dishes. Do I have enough material from 35 mm dishes? ˜1.2 x 10^6 cells.

Read More

Abcam community

Verified customer

Asked on Jul 30 2013

Answer



The buffer used might work but we would strongly suggest using the extraction buffer provided in the kit for the best results. The best way would be to store cell lysates at -80C if needed. The number of cells mentioned in the datasheet are based on our experience with this kit. The customer can use lower number of cells but the RFU value might be low. It is possible to optimize with less cells by using a concentrated sample lysate (that is making the lysate in less volume than recommended).

Read More

Sybille Rex

Abcam Scientific Support

Answered on Jul 30 2013

Question

Hello,

I had a few questions about the Beta Secretase Activity Assay Kit (Fluorometric) (ab65357). I want to make sure that it is the right product for me..

I would like to measure BACE1 activity from CHO cells stably expressing human APP containing the Swedish mutation.

Following the protocol, I can measure the activity of BACE1 using a fraction of the cell lysate without isolating the enzyme?

Importantly, do you have evidence to show that the activity of BACE1 from whole cell lysates (as opposed to just recombinant/isolated BACE1) is reduced upon the addition of beta-secretase inhibitor?







Read More

Abcam community

Verified customer

Asked on May 15 2013

Answer

Thank you for contacting us. This kit does allow you to measure BACE1 from cells without isolating the enzyme. We have tested this protocol and made the protocol from use with cells that were lysed using the kit's extraction buffer.

The publications this kit has been used in are listed below. They can also be found from our online datasheet. Please let me know if you have any further questions.

Jin P et al. Anti-inflammatory and anti-amyloidogenic effects of a small molecule, 2,4-bis(p-hydroxyphenyl)-2-butenal in Tg2576 Alzheimer's disease mice model. J Neuroinflammation 10:2 (2013). Functional Studies ; Mouse . PubMed: 23289709

Kindy MS et al. Deletion of the cathepsin B gene improves memory deficits in a transgenic ALZHeimer's disease mouse model expressing AßPP containing the wild-type ß-secretase site sequence. J Alzheimers Dis 29:827-40 (2012). PubMed: 22337825
Hook G et al. The cysteine protease inhibitor, E64d, reduces brain amyloid-ß and improves memory deficits in Alzheimer's disease animal models by inhibiting cathepsin B, but not BACE1, ß-secretase activity. J Alzheimers Dis 26:387-408 (2011). PubMed: 21613740
Wen L et al. VPS35 haploinsufficiency increases Alzheimer's disease neuropathology. J Cell Biol 195:765-79 (2011). PubMed: 22105352
Cui J et al. Morphine protects against intracellular amyloid toxicity by inducing estradiol release and upregulation of Hsp70. J Neurosci 31:16227-40 (2011). PubMed: 22072674

Read More

Abcam Scientific Support

Answered on May 15 2013

Question

1. In some in-house developed beta-secretase assays, the CSF sample is
pre-incubated in buffer containing sodium acetate, EDTA, CHAPS
deferoxamine mesylate, pepstatin A, and 0.01% BSA at pH 4.5. We would like
to know if any of these compounds could interfere with the components of
the assay?
2. Since the substrate is dissolved in DMSO, would it be possible to
pre-dilute it in Reaction buffer before adding it to the plate, to add
larger volume (eg. 10 or 20 microL instead of 2 microL)

Read More

Abcam community

Verified customer

Asked on Jan 03 2013

Answer

Since this is an enzymatic assay, I would not recommend using a buffer containing EDTA.

Yes, you can add reaction buffer to the substrate. So if you are adding 18 ul of the buffer to 2 ul of the substrate, add only 32 ul of the buffer in the prior step to account for the increased volume in the next step in the protocol.

Read More

Abcam Scientific Support

Answered on Jan 03 2013

Question


we have purchased the Beta secretase Activity Assay Kit with the purpose
of measuring the beta secretase actvitity in our samples. We have
performed the initial testing according to your protocol, but the readings
in the samples were very low,
Regarding the positive control, even though our values were quite
satisfactory (around 27000), would it be better to use PBS instead of
extraction buffer, since we have not used cell lysates?
In the case of very low beta-secretase activity, as in our samples, are
there any changes that can be made to the procedure to get better
sensitivity and higher readings?
Would increasing sample volume be advisable, since the pH of reaction
buffer is in the acidic range, and the buffer cannot be concentrated?
We have tried doubling the incubation time, but with no success.
In addition, in the negative control, we have not obtained desired
inhibition - the readings were higher than in the our samples, and we were
unable to detect the reason for that. Are there any substances in the
biological fluids that could interefere with the inhibitor

Read More

Abcam community

Verified customer

Asked on Nov 29 2012

Answer



Tips to ensure maximum beta secretase activity include:
1. Ensure assay buffer at room temperature
2. Perhaps protein in your sample is inhibiting somehow beta secretase activity. To test this, try spiking active beta secretase control into your samples and compare readings to positive control without your sample, to determine if factors are inhibiting enzymatic activity

Also, I think it would be helpful if you could send along data for review.

Read More

Abcam Scientific Support

Answered on Nov 29 2012

Question

vielen Dank erst einmal für Ihre schnelle und umfassende Antwort.
Ich denke mit dem mir zur Verfügung stehenden Lesegerät (geschlossen und auf 37°C temperierbar) sollte eine Auswertung durchaus möglich sein.
ich werde mich diesbezüglich jedoch erst noch mit meinem Chef beraten müssen.

Read More

Abcam community

Verified customer

Asked on Oct 29 2012

Answer

wenn nach der Beratung mit ihrem Chef weitere Fragen aufkämmen können sie sich gerne nocheinmal melden.

Ich wünsche ihnen weiterhin viel Erfolg mit ihren Experimenten

Read More

Abcam Scientific Support

Answered on Oct 29 2012

Question

Liebe Mitarbeiterin/Lieber Mitarbeiter,

ich möchte im Rahmen meiner Versuche, die ß-Secretase Aktivität bestimmen. Auf der Suche nach einem geeigneten Kit bin ich hierbei über das von ihrer Firma vertriebene "Beta Secretase Activity Assay Kit (Fluorometric) (ab65357)" gestolpert.

Ich habe allerdings eine Frage zu der Probenvermessung.
In der Anleitung zu Ihrem Kit heißt es in Punkt 6: "....incubate in the dark at 37° for 1 hour. 7:Read samples,.........."

Bislang habe ich in einem Anderen Versuchssetting ein a-Secretase-Kit verwendet. In selbigem wurde analog zu Ihrem Kit mit Fluorophor und Quencher gearbeitet. Allerdings konnten die Proben als Zeitverlauf (z.B.: alle 5 min) in einem geeigneten Messgerät vermessen werden.
Ist ein analoges vermessen in dem von Ihnen angebotenen Kit auch problemlos möglich, oder sollte selbiges lieber unterlassen werden?

Read More

Abcam community

Verified customer

Asked on Oct 26 2012

Answer

Vielen Dank für ihre Anfrage.

Für den Versuchsaufbau dieses Kits sollten in jedem Fall immer die positiv und die negativ Kontrollen sowie verschiedene Konzentrationen der Proben gemessen werden. Wenn Sie ein geeignetes Gerät verwenden in welchem die Proben nach Protokoll im Dunkeln inkubiert werden können sollte es möglich sein auch den Zeitverlauf der Reaktion zu vermessen. Das Kit liefert ein optimales Resultat nach der im Protokoll beschriebenen ein stündigen Inkubationszeit. Das ein optimaler Kurvenverlauf bei einer Messung über die Zeit erhalten wird können wir nicht garantieren.

Für die Auswertung ist es wichtig nur die Proben von gleichen Zeitpunkten bezüglich der Konzentration zu vergleichen. Für den Zeitverlauf sollten dementsprechend nur Proben der gleichen Konzentration für die Auswertung verglichen werden.


Ich hoffe diese Information ist hilfreich. Wenn Sie weitere Fragen haben zögern sie nicht sich nocheinmal bei uns zu melden.

Read More

Abcam Scientific Support

Answered on Oct 26 2012

Question


We are interested in purchasing Beta Secretase Activity Assay Kit
(Fluorometric) Cat #ab65357, but have few questions.
Our microplate reader has excitation/emission wavelength combination
355nm/460 or 535nm, which is outside the recommended reading range for
this kit (495-510nm), and we fear it would critically affect tour results.
Do you have any data how reading at different wavelengths affects the
accuracy of the kit, and do you have any suggestions/recommendations how
to deal with our problem?
Are there any publications in which your kit has been used for measurement
of beta-secretase activity in CSF, and not in cell lysates?
Best regards,

Read More

Abcam community

Verified customer

Asked on Jul 06 2012

Answer

Thank you for contacting us with your questions about ab65357.

Do you know what the detection bandwidth is on your machine? If the bandwidth is ±20, you can use this wavelength, but if not, then unfortunatelythe difference inwavelengths will affect the reliability of the assay results.

I have looked through the publications that we are aware of in which this kit was used, and I could not find anyreference of using this kit with CSF samples. I am sorry that we do not have more information in this regard.

Please let me know if you have any further questions or if there is anything else that we can do for you, and I'll be happy to help.

Read More

Abcam Scientific Support

Answered on Jul 06 2012

1-10 of 17 Abreviews or Q&A

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