RPRD2 Antibodies

AND RPRD2 ELISA kits, RPRD2 Proteins

Many biological assays use antibodies to detect RPRD2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with RPRD2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop RPRD2 antibodies...

We validate the specificity of these antibodies to RPRD2 by testing them on tissues known to express RPRD2 positively and negatively. Browse below to find the RPRD2 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: SEPTIN9 Next: ATP11A

RPRD2 Infographic by Boster Bio

All RPRD2 Products

Product

Figures

Specificity

Applications

Price

Anti-RPRD2 Antibody

Human, Mouse

ELISA, WB

$380
Cat # A12747
100ul

RPRD2 Overview

Facts about Regulation of nuclear pre-mRNA domain-containing protein 2.

RPRD2 3D structure. Source: alphafold

Regulation of nuclear pre-mRNA domain-containing protein 2 (RPRD2)

Gene Information

Human
Gene Name:	RPRD2
Uniprot:	Q5VT52
Entrez:	23248

Family

Belongs to:

No superfamily

Alternative Names

HSPC099; KIAA0460FLJ32145; regulation of nuclear pre-mRNA domain containing 2; regulation of nuclear pre-mRNA domain-containing protein 2

Molecular Weight

Mass (kDA):
156.02 kDA

Genomic Context


Human

Location:	1q21.2
Sequence:	1; NC_000001.11 (150364111..150476566)

PTMs

Phosphorylation

Research Areas

DNA Repair

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/RPRD2

References

PMID: 22231121 by Ni Z., et al. Control of the RNA polymerase II phosphorylation state in promoter regions by CTD interaction domain-containing proteins RPRD1A and RPRD1B.

PMID: 25489052 by Myklebust L.M., et al. Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects.