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Thermo Fisher Scientific Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/6270)
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Thermo Fisher Scientific

Thermo Fisher Scientific Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/6270)

상품 한눈에 보기

Duchenne 및 Becker 근이영양증 마커인 Dystrophin 단백질을 검출하는 단클론 항체. Western blot, IHC, ICC 등 다양한 응용에 사용 가능. Human 및 Dog 반응성, Mouse 유래 IgG2a 항체. 단백질 A/G 정제, PBS 버퍼 보관.

브랜드
Thermo Fisher Scientific
카테고리
Monoclonal Antibodies
판매단위
pk

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마지막 업데이트 2025. 07. 29. 오전 02:11
Thermo Fisher Scientific 1756-MSM8-P1ABX Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/6270) 1 pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원
재고문의·견적요청 옵션은 실시간 상담으로 납기를 확인해 드립니다 · 연구비 카드 결제 가능

Thermo Fisher Scientific · Thermo Fisher Scientific Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/6270)

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) 2–4 µg/mL

Product Specifications

Specification Description
Species Reactivity Dog, Human
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone DMD/6270
Immunogen Recombinant fragment (around aa1700–2300) of human DMD
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Does not react with Mouse, Xenopus, or Chick.

Target Information

Dystrophin is the 427 kDa protein product of the DMD/BMD gene located on the X chromosome (Xp21). Western blotting and immunohistochemistry are established methods for detecting abnormalities of dystrophin expression in muscle biopsies. Dystrophin abnormalities occur in nearly all patients with DMD/BMD, though genetic mutations may be detected in only about 65% of cases.

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

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