Actin, alpha 1, Skeletal Muscle (ACTA1) Peptid
ACTA1
Reaktivität: Säugetier
Wirt: Synthetic
BP, WB, IHC
Produktnummer ABIN936401
382,12 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach:
Deutschland
Lieferung in 20 bis 27 Werktagen
Kurzübersicht für Actin, alpha 1, Skeletal Muscle (ACTA1) Peptid (ABIN936401)
Target
Actin (ACTA1)
(Actin, alpha 1, Skeletal Muscle (ACTA1))
Spezies
Säugetier
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Protein-Typ
- Synthetic
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Sequenz
- STMKIKIIAP PERKYSVWIG GSILASLSTF QQMWITKQEY DEAGPSIVHR
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Produktmerkmale
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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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Applikationshinweise
- Optimal conditions should be determined by the investigator
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- 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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Handhabung
- Avoid repeated freeze/thaw cycles.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Store at -20 °C long term.
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- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
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Hintergrund
- 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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Molekulargewicht
- 42 kDa
Target
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