Goat Anti-PPP1R12A Antibody

This goat IgG polyclonal antibody was generated against peptide sequence CREDEYKQKYSRTYD from the C Terminus of protein phosphatase 1 regulatory subunit 12A (PPP1R12A) and recognizes human PPP1R12A.

Highlights:

  • Reacts with human PPP1R12A
  • Suitable for Peptide ELISA, Immunohistochemistry, and Immunofluorescence applications
  • Associated with Genitourinary And/Or Brain Malformation Syndrome

Protein phosphatase 1 regulatory subunit 12A (PPP1R12A) interacts with protein phosphatase type 1 catalytic unit (PP1C) and M20/21 to form the trimeric holoenzyme, myosin phosphatase (MP). Myosin phosphatase is a key regulator of cell morphology and motility. Phosphorylation of specific sites on PPP1R12A inhibits its activity with pathogenic variants of the PPP1R12A gene resulitng in a non-functional MP. Diseases associated with PPP1R12A include Genitourinary And/Or Brain Malformation Syndrome.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EB08594
Goat Anti-PPP1R12A Antibody
100ug specific antibody in 200ul In stock
Regular Price:$415.00
On Sale:
Specifications

Product Type: Antibody
Name: Goat Anti-PPP1R12A Antibody
Alternative Name(s): Myosin phosphatase-targeting subunit 1 (Myosin phosphatase target subunit 1), Protein phosphatase myosin-binding subunit, MBS, MYPT1
Accession ID: NP_002471.1, NP_001231919.1, NP_001231921 .1, NP_001137358.1
Antigen: PPP1R12A
Isotype: IgG
Clonality: Polyclonal
Reactivity: Human
Specificity: PPP1R12A
Immunogen: CREDEYKQKYSRTYD
Species Immunized: Goat
Epitope: C Terminus
Purification Method: Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide
Buffer: Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Tested Applications: Pep-ELISA, IHC, IF
Storage: Aliquot and store at -20C. Minimize freezing and thawing.
Shipped: Cold Packs

Documentation
Data

Immunofluorescence and Immunohistochemistry

WB Data

I. Immunofluorescence analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml). II. Immunofluorescence analysis of paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml). III. (4µg/ml) staining of paraffin embedded Human Testis. Heat induced antigen retrieval with citrate buffer pH 6, HRP-staining. IV. Negative control showing staining of paraffin embedded Human Testis with no primary antibody.

References

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