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Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (GT9712)
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Thermo Fisher Scientific

Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (GT9712)

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Lamin A/C 단백질을 인식하는 마우스 모노클로날 항체로 Western blot, ICC/IF, IP에 적합합니다. 인간 시료에 반응하며 농도는 1 mg/mL입니다. 단기 4°C, 장기 -20°C 보관하며 연구용으로 사용됩니다.

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Thermo Fisher Scientific
카테고리
Monoclonal Antibodies
판매단위
pk

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마지막 업데이트 2025. 08. 03. 오후 09:55
Thermo Fisher Scientific MA531474 Lamin A/C Monoclonal Antibody (GT9712) 100 ul pk판매 단위 pk ·
재고 확인 필요
653,000원VAT 포함 718,300원
재고문의·견적요청 옵션은 실시간 상담으로 납기를 확인해 드립니다 · 연구비 카드 결제 가능

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (GT9712)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000
Immunoprecipitation (IP) 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone GT9712
Immunogen Recombinant protein encompassing a sequence within the center region of human Lamin A/C
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains No preservative
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)
RRID AB_2787106

Product Specific Information

  • Keep as a concentrated solution.
  • Predicted reactivity: Mouse (87%), Rat (92%), Dog (96%), Pig (96%), Rhesus Monkey (99%), Chimpanzee (100%)
  • Positive Control: HeLa, HeLa nuclear
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Lamins are intermediate filament proteins forming a matrix on the inner surface of the nuclear envelope. These proteins exist in three forms (A, B, and C) and are found in many cell types.
Lamins A and C are alternatively spliced products of the LMNA gene.
Mutations in LMNA are associated with several disorders, including:

  • Emery-Dreifuss muscular dystrophy
  • Dunnigan-type familial partial lipodystrophy (FPLD)
  • Limb-girdle muscular dystrophy (LGMD1B)
  • Dilated cardiomyopathy (CMD1A)
  • Axonal neuropathy (Charcot-Marie-Tooth disease; CMT2B1)
  • Mandibuloacral dysplasia (MAD)

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

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