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Thermo Fisher Scientific Actin alpha 1, Skeletal Muscle Monoclonal Antibody (ACTA1/360)
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Thermo Fisher Scientific Actin alpha 1, Skeletal Muscle Monoclonal Antibody (ACTA1/360)

상품 한눈에 보기

사람 유래 ACTA1 단백질을 인식하는 단클론 항체로, 골격근 알파 액틴 검출에 적합합니다. Western blot, IHC, ICC, Flow Cytometry 등 다양한 응용에 사용 가능하며, 단백질 A/G 정제 및 액상 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

카탈로그번호
58-MSM1-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 02. 오후 07:10
Thermo Fisher Scientific 58-MSM1-P1 Actin alpha 1, Skeletal Muscle Monoclonal Antibody (ACTA1/360) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원
Thermo Fisher Scientific 58-MSM1-P0 Actin alpha 1, Skeletal Muscle Monoclonal Antibody (ACTA1/360) 20 ug pk판매 단위 pk ·
재고 확인 필요
449,700원VAT 포함 494,670원

Thermo Fisher Scientific · Thermo Fisher Scientific Actin alpha 1, Skeletal Muscle Monoclonal Antibody (ACTA1/360)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10⁶ cells

Product Specifications

Specification Detail
Species Reactivity Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone ACTA1/360
Immunogen Recombinant human ACTA1 protein
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)

Product Specific Information

Predicted to show a broad reactivity.

Target Information

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved and play essential roles in cell motility, structure, and integrity. Alpha, beta, and gamma actin isoforms have been identified — alpha actins are major constituents of the contractile apparatus, while beta and gamma actins regulate cell motility. This actin is an alpha actin found in skeletal muscle. Mutations in this gene are associated with 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.

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

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