Ppp1r21 Antibodies

AND Ppp1r21 ELISA kits, Ppp1r21 Proteins

Many biological assays use antibodies to detect Ppp1r21, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Ppp1r21 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Ppp1r21 antibodies...

We validate the specificity of these antibodies to Ppp1r21 by testing them on tissues known to express Ppp1r21 positively and negatively. Browse below to find the Ppp1r21 antibody that suites your experiment. We have 3 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.

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Ppp1r21 Infographic by Boster Bio

All Ppp1r21 Products

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Product

Figures

Specificity

Applications

Price

KLRAQ (PPP1R21) (NM_152994) Human Recombinant Protein

Coomassie blue staining of purified PPP1R21 protein

$1062
Cat # PROTQ6ZMI0
20 µg

KLRAQ (PPP1R21) (NM_152994) Human Over-expression Lysate

Human

$960
Cat # LS129285
20 µg, 100 µg

Anti-PPP1R21 Antibody

Human, Mouse

ELISA, IF, IHC, WB

$370
Cat # A15058-1
100 μl/vial

Ppp1r21 Overview

Facts about Protein phosphatase 1 regulatory subunit 21.

Protein phosphatase 1 regulatory subunit 21 (Ppp1r21)

Gene Information

Mouse
Gene Name:	Ppp1r21
Uniprot:	Q3TDD9
Entrez:	73825

Family

Belongs to:

No superfamily

Alternative Names

CCDC128; coiled-coil domain containing 128; Coiled-coil domain-containing protein 128; FLJ16566; KLRAQ motif containing 1; KLRAQ motif-containing protein 1; MGC111781

Molecular Weight

Mass (kDA):
88.338 kDA

Genomic Context


Mouse

Location:	17\|17 E4
Sequence:	17;

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Ppp1r21

References

PMID: 30520571 by Rehman A.U., et al. Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.