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Thermo Fisher Scientific Actin, Muscle Specific (Muscle Cell Marker) Monoclonal Antibody (MSA/953)
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Thermo Fisher Scientific Actin, Muscle Specific (Muscle Cell Marker) Monoclonal Antibody (MSA/953)

상품 한눈에 보기

근육 특이적 액틴 단백질을 인식하는 단일클론 항체로, 근육세포 마커 연구용에 적합. Western blot 및 면역조직화학(IHC) 분석에 사용 가능. 인간, 토끼, 쥐 시료 반응성. 단백질 A/G 정제 및 액상 형태로 제공. 연구용 한정 제품.

카탈로그번호
MSM2-953-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 04. 오후 08:06
Thermo Fisher Scientific MSM2-953-P1 Actin, Muscle Specific (Muscle Cell Marker) Monoclonal Antibody (MSA/953) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원
Thermo Fisher Scientific MSM2-953-P0 Actin, Muscle Specific (Muscle Cell Marker) Monoclonal Antibody (MSA/953) 20 ug pk판매 단위 pk ·
재고 확인 필요
449,700원VAT 포함 494,670원

Thermo Fisher Scientific · Thermo Fisher Scientific Actin, Muscle Specific (Muscle Cell Marker) Monoclonal Antibody (MSA/953)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.5–1.0 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 0.5–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Rabbit, Rat
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone MSA/953
Immunogen Synthetic peptide common among human muscle actins
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C, do not freeze
Shipping Conditions Ambient (domestic); Wet ice (international)

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 in muscle
  • Beta and gamma actins: Involved in regulation of cell motility

This antibody targets alpha actin, found in skeletal muscle.
Mutations in this gene are associated with:

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

These conditions are characterized by muscle fiber defects.


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

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