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MilliporeSigma

CS0030

Sigma-Aldrich

Senescence Cells Histochemical Staining Kit

sufficient for 100 tests

Synonym(s):

Senescent cells IHC kit, cellular β-galactosidase probe

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$428.00

$428.00


Estimated to ship onJuly 07, 2025FromSAINT LOUIS


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1 KIT
$428.00

About This Item

UNSPSC Code:
12352207
NACRES:
NA.32

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$428.00


Estimated to ship onJuly 07, 2025FromSAINT LOUIS


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Need help? Our team of experienced scientists is here for you.
Let Us Assist

usage

sufficient for 100 tests

Quality Level

packaging

pkg of 1 kit

storage condition

dry at room temperature

detection method

colorimetric

shipped in

dry ice

storage temp.

−20°C

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This Item
GALSKAA002SCT210
usage

sufficient for 100 tests

usage

 kit sufficient for 100 tests (using a 3.5 cm dish)

usage

-

usage

-

packaging

pkg of 1 kit

packaging

-

packaging

-

packaging

-

storage condition

dry at room temperature

storage condition

-

storage condition

-

storage condition

-

detection method

colorimetric

detection method

-

detection method

colorimetric

detection method

fluorometric

shipped in

dry ice

shipped in

dry ice

shipped in

wet ice

shipped in

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

storage temp.

-

General description

The Senescence Cells Histochemical Staining Kit contains all the reagents required for identifying senescent cells using an assay based on a histochemical stain for β-galactosidase activity at pH 6. β-galactosidase activity is detectable in senescent cells, but not in quiescent, immortal, or tumor cells. Cellular senescence is a progression of events, whereby cells move from an actively dividing to a non-dividing stage. The cellular senescence process is associated with aging. The decrease in cell division is virtually irreversible and complete. In conjunction with the loss of the ability to divide, changes occur in the morphology, shape, and physical appearance of the cells, and their pattern of gene expression. At the end of the process cell death usually occurs, although the cells may remain viable for a long time.

Application

Senescence Cells Histochemical Staining Kit has been used for:
  • senescence-associated β-galactosidase assay
  • to test for senescence in human pancreatic cancer cells
  • adipose-derived stem cells (ADSCs)
  • cord blood mesenchymal stromal/stem cells (CBMSC)

Biochem/physiol Actions

Replicative senescence is a growth-arrest state associated with loss of division potential, changes in cell morphology, shape and physical appearance, and the pattern of gene expression in cells.

Legal Information

Manufactured under license to US Patent Nos. 5,491,069 and 5,795,728.

Kit Components Only

Product No.
Description

  • X-gal solution 4 mL

  • Staining Solution, 10X 15 mL

  • Fixation Buffer 10x 15 mL

  • Reagent B 1.5 mL

  • Reagent C 1.5 mL

  • Dulbecco's Phosphate Buffered Saline (PBS) 10x 60 mL

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Dam. 1 - Muta. 2 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects


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Questions

1–8 of 8 Questions  
  1. Can this kit be used to stain FFPE sections?

    1 answer
    1. This kit has not been validated for compatibility with formalin-fixed paraffin-embedded (FFPE) tissue sections. It is designed for cultured cells and advises against using ethanol- or methanol-based fixatives, as these can inactivate the β-galactosidase label critical for senescence detection. FFPE processing typically involves ethanol or reagent-grade alcohol (primarily ethanol with minor methanol and isopropyl alcohol components) during dehydration, which suggests potential incompatibility with the kit’s staining mechanism. Consequently, this kit is likely not suitable for FFPE-processed tissues without protocol optimization, e.g., alternative fixation methods or additional validation to ensure compatibility.

      Helpful?

  2. Can we use confocal/basic fluorescent microscope for capturing the expression of Beta Galactosidase after using this staining kit?

    1 answer
    1. This kit has not been tested for use with confocal or fluorescent microscopes. X-gal staining does not involve a specific wavelength and it would be up to the end user to determine suitability. Note below, in a previously submitted question, that this kit has not been tested for dual staining with fluorescent dyes.

      Helpful?

  3. Does kit CS0030 include a counterstain?

    1 answer
    1. No, the CS0030 kit does not include a counterstain.

      Helpful?

  4. Is there a method to extract the stain from cells when using the Senescence Cells Histochemical Staining Kit (Catalog Number CS0030) for cells in transwell inserts where cell counting is not feasible?

    1 answer
    1. The CS0030 kit is intended for cell visualization using a microscope and does not include a specific procedure for dye extraction from cells.

      Helpful?

  5. Is there a protocol for staining HCHO-fixed tissue culture cells, specifically for cells growing on coverslips or slides?

    1 answer
    1. For staining purposes, there is no significant difference between staining wells attached to a culture plate or cells attached to a coverslip or glass slide. The primary difference lies in the amount of reagent required for the staining. It is advisable to ensure adequate coverage of the cells, and the insert contains a table that provides guidance on the amount of reagent required for staining.

      Helpful?

  6. I have been using it well for a long time. thank you I want to stain beta-gal staining and apoptosis-related IF together. Is there a recommended order or method?

    1 answer
    1. The CS0030 kit has not been tested for use in dual staining, it would be up to the end user to determine suitability. There are several factors to consider with regard to attempting this modification.
      1. The CS0030 includes a fixation step. Cells are not viable at the time of staining. Therefore any 'live cell' fluorescent stain would not be suitable following fixation.
      2. There is an incubation period of 2 hours to overnight. This may deplete or cause certain fluorescent dyes to fade which would mean a 'one-time use' for visualizing the IF-stained cells.
      3. The staining mechanism for CS0030 is pH dependent. This may not be suitable for some fluorescent dyes.
      4. One possible robust fluorescent stain to consider would be DAPI, which could be applied following the b-gal staining. DAPI will stain fixed cells and can be preserved if stored in the dark.

      To discuss further, please navigate to the link https://www.sigmaaldrich.com/techservice, and click on "Product Technical Inquiries" under the Products Section with all the required information so that a member of the Technical Service team can reach out to assist further.

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  7. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  8. Can Product CS0030, Senescence Cells Histochemical Staining Kit be used with fixed cells/tissues?

    1 answer
    1. Product CS0030, Senescence Cells Histochemical Staining Kit was designed for use with fresh (not-fixed) cells.  The kit contains a fixation buffer to fix the cells.  It is 10% formaldehyde, 1% glutaraldehyde in DPBS at 1X.  The cells will be fixed prior to staining.  The staining will show the beta-galactosidase activity that was present at the time of fixation.We tested the kit only on cells and we have no experience with tissue sections. The following papers use an assay for ßGAL on tissue sections which suggests that the kit will work with tissue sections.Castro P, et al., Interleukin-8 expression is increased in senescent prostatic epithelial cells and promotes the development of benign prostatic hyperplasia. Prostate, 60(2), 153-159 (2004).Chen, Z., et al., Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis. Nature, 436, 725-730 (2005).

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