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Thermo Fisher Scientific Actin, Skeletal Muscle Polyclonal Antibody
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Thermo Fisher Scientific Actin, Skeletal Muscle Polyclonal Antibody

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Rabbit polyclonal antibody targeting skeletal muscle actin (ACTA1). Validated for WB and IHC applications. Recognizes cytoplasmic actin in skeletal muscle tissues. Supplied as liquid, unconjugated form, purified by antigen affinity chromatography. For ...

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pk
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ADBIX 2026 전시회10/28~30 코엑스 · 사전등록 안내자세히보기
Thermo Fisher Scientific 500-3884 Actin, Skeletal Muscle Polyclonal Antibody 100 ug pk판매 단위 pk
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346,100원VAT 포함 380,710원

Thermo Fisher Scientific · Thermo Fisher Scientific Actin, Skeletal Muscle Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.1–1 µg/mL

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 2–10 µg/mL

Product Specifications

항목 내용
Species Reactivity Guinea pig, Human, Rabbit, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide derived from N-terminus of human alpha skeletal muscle isoforms of actin (ACTA1, UniProt ID: P68133-1)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with proprietary stabilizer
Contains 0.01% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Positive control: Skeletal muscle
  • Cellular location: Cytoplasmic

Target Information

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved and play key roles in cell motility, structure, and integrity. Alpha, beta, and gamma actin isoforms have been identified:

  • Alpha actins: major constituent of the contractile apparatus
  • Beta and gamma actins: involved in regulation of cell motility

This actin is an alpha actin found in skeletal muscle.
Mutations in this gene cause:

  • Nemaline myopathy type 3
  • Congenital myopathy with excess of thin myofilaments
  • Congenital myopathy with cores
  • Congenital myopathy with fiber-type disproportion

These diseases lead to muscle fiber defects.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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