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Mouse Anti-Bovine Nucleophosmin (B23) Monoclonal Antibody

Cat. No.VD8N50

Product TypeAnimal-targeted Antibodies

Size

Product Overview

BioVenic mouse monoclonal antibody is specific for bovine nucleophosmin. It can be applied to WB, IF and ICC assays of bovine nucleophosmin.

Specifications

Application WB; IF; ICC
Clonality Monoclonal
Classification Primary Antibody
Clone G3N14
Host Mouse
Target Species Bovine
Species Reactivity Bovine
Specificity Bovine Nucleophosmin
Isotype IgG
Immunogen Purified recombinant bovine B23 protein fragments
Concentration 1 mg/mL
Conjugation Unconjugated
Physical State Liquid

Target Information

B23, or nucleophosmin (NPM1), is an abundant nucleolar protein that plays a critical role in the maintenance of genomic stability and regulation of apoptosis. It is implicated in several pathways, such as mRNA transport, chromatin remodeling, and cell proliferation. NPM1 functions not only as a proto-oncogene but also has been reported to act as a tumor suppressor. Its multifunctional role within the cell makes it a significant player in various DNA repair pathways. NPM1 is also involved in the regulation of rRNA synthesis and serves as a histone chaperone, participating in chromatin remodeling and transcription regulation. Mutations and dysregulation of NPM1 have been associated with several types of cancer, making it a target of interest for cancer research and potential therapeutic intervention .

Target Bovine Nucleophosmin
Target Synonym NPM1
Gene ID 614028
UniProt ID Q3T160

Shipping and Storage

This product is shipped with ice gel packs. Store at -20°C (up to 12 months) on receipt. Avoid repeated freezing and thawing as this may denature the antibody.

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Box, Joseph K., et al. "Nucleophosmin: from structure and function to disease development." BMC molecular biology 17 (2016): 1-12.
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