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GERPN202

Anti-Brdu Antibody

Cytiva RPN202

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

conjugate

unconjugated

antibody product type

primary antibodies

packaging

pkg of 130 μL

manufacturer/tradename

Cytiva RPN202

storage temp.

2-8°C

General description

The Anti-Bromodeoxyuridine Antibody is supplied in the same formulation as the monoclonal antibody to BrdU in the kit. The antibody/nuclease mixture is compatible with detection systems that incorporate fluorescently labeled antibodies and biotin-streptavidin detection reagents.

Features and Benefits

  • The monoclonal antibody to Bromo-deoxyuridine is supplied in the.same formulation used in the Cytiva Cell Proliferation Kit (RPN20).
  • No need for chemical denaturation.
  • Detection while maintaining cell morphology.
  • Double immunocytochemical staining studies can be perfromed.

Storage and Stability

Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.

Analysis Note

To view the Certificate of Analysis for this product, please visit www.cytiva.com.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Health hazard

signalword

Danger

hcodes

Storage Class

13 - Non Combustible Solids


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Samir A Bello et al.
Journal of marine science and engineering, 10(2) (2022-10-27)
The cellular events underlying intestine regrowth in the sea cucumber Holothuria glaberrima have been described by our group. Currently, the molecular and signaling mechanisms involved in this process are being explored. One of the limitations to our investigations has been

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