Dystrophia Myotonica-Protein Kinase (DMPK) (Middle Region) Peptide
DMPK
Reactivité: Humain
Hôte: Synthetic
BP, IHC, WB
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- Antigène Tous les produits DMPK
- DMPK (Dystrophia Myotonica-Protein Kinase (DMPK))
- Protein Region
- Middle Region
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-DMPK antibody (Catalog #: ARP42183_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- DMPK (Dystrophia Myotonica-Protein Kinase (DMPK))
- Synonymes
- DMPK Peptide, DM Peptide, DM1 Peptide, DM1PK Peptide, DMK Peptide, MDPK Peptide, MT-PK Peptide, Dm15 Peptide, DM1 protein kinase Peptide, dystrophia myotonica-protein kinase Peptide, DMPK Peptide, Dmpk Peptide
- Sujet
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The protein encoded by this gene is a serine-threonine kinase that is closely related to other kinases that interact with members of the Rho family of small GTPases. Substrates for this enzyme include myogenin, the beta-subunit of the L-type calcium chann
Alias Symbols: DM, DM1, DM1PK, DMK, MDPK, MT-PK
Protein Interaction Partner: CELF1,RARG,SP1,PPP1R12A,ATN1,ATXN1,CELF1,FXYD1,GABARAP,HSPB2,PLN,PPP1R12A,RAF1,UBQLN4,HSPB2,RAC1
Protein Size: 629 - Poids moléculaire
- 69 kDa
- ID gène
- 1760
- NCBI Accession
- NM_004409, NP_004400
- UniProt
- Q09013
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