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Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (JE51-60)
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Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (JE51-60)

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Thermo Fisher의 Lamin A/C Recombinant Rabbit Monoclonal Antibody (JE51-60)은 인간 Lamin A/C 단백질을 인식하는 항체로, WB, IHC, ICC, Flow Cytometry에 최적화되어 있습니다. 고순도 단백질 A 정제, 안정적 액상 포맷, 연구용으로 다양한 조직 샘플에 적용 가능합니다.

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마지막 업데이트 2025. 07. 29. 오후 10:36
Thermo Fisher Scientific MA534874 Lamin A/C Recombinant Rabbit Monoclonal Antibody (JE51-60) 100 ul pk판매 단위 pk ·
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594,400원VAT 포함 653,840원

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (JE51-60)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:1000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:2000
Immunocytochemistry (ICC/IF) 1:200
Flow Cytometry (Flow) 1:1000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone JE51-60
Immunogen Recombinant protein within Human Lamin A/C (aa 191–309)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer TBS, pH 7.4, with 0.05% BSA, 40% glycerol
Contains 0.05% sodium azide
Storage Conditions -20°C, avoid freeze/thaw cycles, store in dark
Shipping Conditions Wet ice
RRID AB_2848782

Product Specific Information

Positive Control:
A549 cell, A431, SiHa, rat testis tissue, human tonsil tissue, human colon carcinoma tissue, human breast tissue, human gastric carcinoma tissue, mouse brain tissue, Hela.

Target Information

Lamins are intermediate filament proteins forming a network on the inner surface of the nuclear envelope. They exist in three main forms (A, B, and C) and are expressed in various cell types. Lamins A and C are alternatively spliced variants of the LMNA gene.
Mutations in LMNA are associated with multiple 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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