This purified recombinant mouse monoclonal antibody recognizes TDRD3 in human samples.

Recombinant antibody characteristics include:

• Validation in Immunoprecipitation
• Superior lot-to-lot consistency
• Extremely high specificity and sensitivity
• Recombinant mouse monoclonal antibody
• Specific for TDRD3

Tudor domain-containing protein 3 (TDRD3) is a 73 kD protein. It requires an intact tudor domain to act as a transcriptional coactivator. It can interact with arginine-methylated polypeptides and primarily localizes to the cytoplasm. When cells are subjected to stress, TDRD3 has been shown to accumulate in stress granules (1).

Exceptional Consistency Saves You Time and Money
Recombinant antibodies are produced by transfection of mammalian cells with heavy and light chain antibody cDNAs. This provides you with the highest consistency between lots, eliminating the need to revalidate your assays for each lot.

High Specificity Means More Reliable Data
The recombinant technology employed in manufacture of the antibody assures greatest degree of reliability. Staining of nonspecific proteins is virtually eliminated while very high sensitivity is achieved. Life Technologies has validated this antibody in immunoprecipitation.

High Sensitivity Lets You Detect Low Levels of Target Protein
Recombinant antibodies demonstrate much higher sensitivity than ordinary antibodies. Proteins expressed in low levels can be detected with high specificity allowing you to use less of your precious samples than with ordinary antibodies.

Recombinant mouse IgG – Use Like Any Other IgG Antibody
As with traditional IgG antibodies, gel electrophoresis of recombinant antibodies produces a 150 kDa band under non-reducing conditions and 50 kDa and 25 kDa bands under reducing conditions.

For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.

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References:

  1. Isabelle Goulet, Sophie Boisvenue, Sophie Mokas, Rachid Mazroui, Jocelyn Côté. TDRD3, a novel Tudor domain-containing protein, localizes to cytoplasmic stress granules, 2008 Hum Mol Genet. 17(19): 3055-3074