Actin, alpha 1, Skeletal Muscle (ACTA1) (C-Term) Peptid
ACTA1
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle Actin (ACTA1) Produkte
- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
- Protein Region
- C-Term
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- STMKIKIIAP PERKYSVWIG GSILASLSTF QQMWITKQEY DEAGPSIVHR
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-ACTA1 Antibody. 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.
- Aufreinigung
- Purified
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-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
- Hintergrund
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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.
Alias Symbols: ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3
Protein Interaction Partner: ABL1,ACTA1,ACTR10,ACTR1B,ADSS,AFAP1,AIF1,CCIN,CCT4,CCT5,CFL1,CLIC5,CNN1,CORO2B,COTL1,CTNND1,CTTN,CYFIP1,CYTH1,DLG1,DMD,DNASE1,DNMBP,DTNA,EGFR,EPB41,EPB41L2,EPS8,FGD4,FHOD1,FSCN1,GAS2,GAS7,GC,GSN,HCLS1,HIP1R,IQGAP1,ITGA2,ITPKA,JUB,KIF23,KLHL20,LASP1,MACF1,
Protein Size: 377 - Molekulargewicht
- 42 kDa
- Gen-ID
- 58
- NCBI Accession
- NM_001100, NP_001091
- UniProt
- P68133
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