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Thermo Fisher Scientific Actin Muscle Monoclonal Antibody (MSA06 (HUC1-1))
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Thermo Fisher Scientific Actin Muscle Monoclonal Antibody (MSA06 (HUC1-1))

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Actin Muscle Monoclonal Antibody (MSA06, HUC1-1)은 alpha-smooth, skeletal, cardiac muscle actin을 인식하는 pan muscle 항체입니다. Western blot과 IHC에 적합하며, 다양한 근육 및 종양 연구에 활용됩니다. 4°C 보관, 액상 형태, 연구용 전용 시약입니다.

카탈로그번호
MA511874
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오전 06:23
Thermo Fisher Scientific MA511874 Actin Muscle Monoclonal Antibody (MSA06 (HUC1-1)) 500 ul pk판매 단위 pk ·
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573,900원VAT 포함 631,290원

Thermo Fisher Scientific · Thermo Fisher Scientific Actin Muscle Monoclonal Antibody (MSA06 (HUC1-1))

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1–3 µg/mL View 1 publication
Immunohistochemistry (IHC) View 3 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:100 View 1 publication

Product Specifications

Item Description
Published species Fish, Mouse, Zebrafish
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone MSA06 (HUC1-1)
Immunogen Purified actin
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Storage conditions 4°C
Shipping conditions Wet ice
RRID AB_10989678

Product Specific Information

This antibody reacts with alpha-smooth muscle, alpha-skeletal, and alpha-cardiac (sarcomeric) actins. It serves as a pan muscle actin antibody and reacts with tumors arising from smooth muscle (leiomyosarcomas) as well as skeletal muscle tumors (rhabdomyosarcomas).


Target Information

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

  • Alpha actins: Major constituents 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 several congenital myopathies, including nemaline myopathy type 3, congenital myopathy with excess thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion—conditions that 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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