Actin, alpha 1, Skeletal Muscle (ACTA1) Peptide
ACTA1
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
N° du produit ABIN936401
382,12 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination:
France
Envoi sous 20 à 27 jours ouvrables
Aperçu rapide pour Actin, alpha 1, Skeletal Muscle (ACTA1) Peptide (ABIN936401)
Antigène
Actin (ACTA1)
(Actin, alpha 1, Skeletal Muscle (ACTA1))
Origine
Mammifères
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Type de proteíne
- Synthetic
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Séquence
- STMKIKIIAP PERKYSVWIG GSILASLSTF QQMWITKQEY DEAGPSIVHR
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Attributs du produit
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A synthetic peptide for use as a blocking control in assays to test for specificity of ACTA1 antibody,
Alternative Names: ACTA1 control peptide, ACTA1 antibody Blocking Peptide, Anti-ACTA1 Blocking Peptide, actin, alpha 1, skeletal muscle Blocking Peptide, ACTA Blocking Peptide, ASMA Blocking Peptide, CFTD Blocking Peptide, CFTD1 Blocking Peptide, CFTDM Blocking Peptide, MPFD Blocking Peptide, NEM1 Blocking Peptide, NEM2 Blocking Peptide, NEM3 Blocking Peptide, ACTA1, ACTA-1, ACTA 1, ACTA-1 Blocking Peptide, ACTA 1 Blocking Peptide
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Indications d'application
- Optimal conditions should be determined by the investigator
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
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Buffer
- PBS
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Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20 °C long term.
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- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
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Sujet
- The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.
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Poids moléculaire
- 42 kDa
Antigène
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