Validation Data Gallery
Tested Applications
Positive WB detected in | mouse skin tissue, HEK-293 cells, A431 cells, PC-3 cells |
Recommended dilution
Application | Dilution |
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Western Blot (WB) | WB : 1:5000-1:50000 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Product Information
85217-4-RR targets Plakophilin 1 in WB, ELISA applications and shows reactivity with human, mouse samples.
Tested Reactivity | human, mouse |
Host / Isotype | Rabbit / IgG |
Class | Recombinant |
Type | Antibody |
Immunogen | Plakophilin 1 fusion protein Ag18153 相同性解析による交差性が予測される生物種 |
Full Name | plakophilin 1 (ectodermal dysplasia/skin fragility syndrome) |
Calculated molecular weight | 747 aa, 83 kDa |
Observed molecular weight | 70-75 kDa |
GenBank accession number | BC114571 |
Gene Symbol | PKP1 |
Gene ID (NCBI) | 5317 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein A purification |
UNIPROT ID | Q13835 |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol{{ptg:BufferTemp}}7.3 |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
Background Information
Plakophilin 1, also known as PKP1, B6P, is a member of the arm-repeat protein family. PKP1 contains arm-repeat (armadillo) domains, localizes to nuclei and cell desmosomes, and participates in linking cadherins to intermediate filaments in the cytoskeleton (PMID: 10747098). PKP1 contributes to epidermal morphogenesis and facilitates the formation of intermediate filaments. Mutations in PKP1 have been associated with the ectodermal dysplasia/skin fragility syndrome (PubMed:9326952, 10852826).
Protocols
Product Specific Protocols | |
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WB protocol for Plakophilin 1 antibody 85217-4-RR | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |