prk-2 Antibody

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Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
prk-2 antibody; F45H7.4 antibody; Serine/threonine-protein kinase prk-2 antibody; EC 2.7.11.1 antibody; PIM-related kinase 2 antibody
Target Names
prk-2
Uniprot No.

Target Background

Function
The prk-2 antibody targets a protein involved in the negative regulation of synaptic differentiation in PLM neurons.
Database Links

KEGG: cel:CELE_F45H7.4

STRING: 6239.F45H7.4.1

UniGene: Cel.17141

Protein Families
Protein kinase superfamily, Ser/Thr protein kinase family, PIM subfamily

Q&A

PRK2 (Protein Kinase C-Related Kinase 2) antibodies are critical tools for studying cellular signaling, cancer biology, and kinase regulation. Below are methodologically focused FAQs addressing both foundational and advanced research considerations, supported by experimental evidence from peer-reviewed studies and technical validations.

Advanced Research Questions

How to resolve contradictory phosphorylation data in PRK2 activation studies?

  • Context-dependent analysis: PRK2 phosphorylation at Thr816/Thr958 varies by cellular stress (e.g., serum starvation vs. growth factor stimulation) .

  • Kinase profiling: Pair antibody-based detection with pharmacological inhibitors (e.g., Y27632) to rule out cross-reactivity with Rho-associated kinases .

What functional assays link PRK2 antibody data to cancer therapeutic outcomes?

  • Proliferation assays: In TNBC models (e.g., BT-549, HCC-1395), PRK2 depletion reduces growth by 40–60% .

  • In vivo validation: Use syngeneic mouse models (e.g., MET1 cells) with PRK2-KO and rescue experiments (PRK2:GFP) :

ModelPRK2 StatusProliferation RateCitation
MET1 (mouse)KO↓ 55%
MET1 + PRK2Rescue↔ Wild-type

How to design co-depletion studies investigating PRK2/PRK1 functional redundancy?

  • siRNA combinations: Co-target PRK1 and PRK2 in serum-starved cells to assess AKT/ERK pathway crosstalk .

  • Phenotypic readouts:

    • Enhanced pAKT (Ser473/Thr308) in dual knockdowns vs. single depletion .

    • Spheroid growth defects in 3D cultures (mIMCD3 cells) .

Methodological Best Practices

Key antibody performance metrics across studies:

ApplicationRecommended DilutionCell/Model SystemCritical ControlsCitation
Western Blot1:5,000–1:10,000HeLa, MET1 TNBCPRK2-KO lysates, peptide blocking
IHC1:100–1:200Prostate/lung cancerIsotype-matched IgG, FFPE blocks
Flow Cytometry1:200–1:400NIH/3T3, HeLaPermeabilization validation

Data Conflict Resolution Framework

  • Cross-platform validation: Correlate antibody data with Depmap CRISPR screens (e.g., PRK2 sensitivity scores in TNBC) .

  • Phospho-specificity: Use λ-phosphatase treatment to confirm phosphorylation-dependent signals .

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