Actin, alpha 1, Skeletal Muscle (ACTA1) Peptide
ACTA1
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
Catalog No. ABIN936319
Quick Overview for Actin, alpha 1, Skeletal Muscle (ACTA1) Peptide (ABIN936319)
Target
Actin (ACTA1)
(Actin, alpha 1, Skeletal Muscle (ACTA1))
Origin
Mammalian
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Peptide Type
- Synthetic
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Sequence
- GQKDSYVGDE AQSKRGILTL KYPIEHGIIT NWDDMEKIWH HTFYNELRVA
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Characteristics
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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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Application Notes
- 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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Handling Advice
- Avoid repeated freeze/thaw cycles.
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Storage
- -20 °C
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Storage Comment
- Store at -20 °C long term.
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- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
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Background
- 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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Molecular Weight
- 42 kDa
Target
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