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11170376001

Roche

Anti-Bromodeoxyuridine

from mouse IgG1 (clone: BMC9318)

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Synonym(s):
anti-BrdU, antibody

biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

BMC9318, monoclonal

assay

90% (HPLC and SDS-PAGE)

form

solution

packaging

pkg of 50 μg (500 μl)

manufacturer/tradename

Roche

isotype

IgG1

storage temp.

−20°C

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This Item
B2531MAB3262BSAB4700630
vibrant-m

11170376001

Anti-Bromodeoxyuridine

clone

BMC9318, monoclonal

clone

BU-33, monoclonal

clone

PRB-1, monoclonal

clone

MoBu-1, monoclonal

conjugate

unconjugated

conjugate

unconjugated

conjugate

biotin conjugate

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody form

ascites fluid

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

packaging

pkg of 50 μg (500 μl)

packaging

-

packaging

-

packaging

-

form

solution

form

-

form

-

form

buffered aqueous solution

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General description

Anti-Bromodeoxyuridine is a monoclonal antibody to 5-bromo-2′-deoxyuridine-5′-monophosphate.

Specificity

The antibody specifically binds to bromodeoxyuridine and crossreacts with iodouridine (10%). Anti-bromo-deoxyuridine does not crossreact with fluorodeoxy-uridine, nor with any endogenous cellular components such as thymidine or uridine.

Immunogen

The epitope is apparently inside the DNA helix. DNA has to be denatured to ssDNA before antibody efficiently binds to DNA-BrdU.

Application

Anti-bromodeoxyuridine (Anti-BrdU) antibody is suitable for monitoring proliferating cells in blood, tissues, and tumors, as well as for determining BrdU incorporation on a single-cell level using:
  • Flow cytometry
  • Immunohistocytochemistry
  • Cryosections
  • Paraffin sections

Quality

The antibody is ≥90% pure as determined by SDS-PAGE with Coomassie-blue staining, and by HPLC.

Specifications

Preparation: BALB/c mice were immunized with a bromodeoxyuridine-bovine serum albumin conjugate. Lymphocytes isolated from the spleen were fused with Ag8.653 myeloma cells to create the BMC 9318 clone. The antibody was produced in ascites in BALB/c mice and purified by ion-exchange chromatography.
No. of tests: 250 (Flow cytometry)

Physical form

Solution, stabilized with phosphate buffered saline, pH 7.4, containing 0.09% (w/v) sodium azide and 0.2% (w/v) gelatin.

Preparation Note

Working concentration: Flow cytometry: 2 μg/ml (0.2 μg/100 μl/106 cells); Immunohistocytochemistry: 6 μg/ml
Working concentration of conjugate depends on application and substrate. Dilutions should be made in PBS (pH 7.4) containing 0.1% BSA to maintain stability of the antibody.

Analysis Note

Anti-Bromodeoxyuridine shows 10% cross reaction with iodo-deoxyuridine, but no cross reaction to fluoro-deoxyuridine.
No cross reaction to any endogenous thymidine or uridine.
Cross reactivity with 5-Br-UTP has not been tested but it is suggested that there is a good chance for reaction, because the only difference is an absent hydroxyl group on the ribose distal to the bromine substitution.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Storage Class

12 - Non Combustible Liquids

wgk_germany

nwg

flash_point_f

No data available

flash_point_c

No data available


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American journal of physiology. Renal physiology, 297(3), F809-F815 (2009-06-19)
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