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Thermo Fisher Scientific Lamin A/C Polyclonal Antibody
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Thermo Fisher Scientific Lamin A/C Polyclonal Antibody

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Lamin A/C 단백질을 인식하는 Rabbit Polyclonal Antibody로 인간, 마우스, 랫트에 반응. Western blot, IHC, ICC/IF, IP 등 다양한 응용에 적합. 고순도 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공.

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마지막 업데이트 2025. 08. 05. 오후 04:05
Thermo Fisher Scientific PA578042 Lamin A/C Polyclonal Antibody 100 ul pk판매 단위 pk ·
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712,600원VAT 포함 783,860원

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Polyclonal Antibody

Thermo Fisher Scientific Lamin A/C Polyclonal Antibody

Applications and Tested Dilution

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

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein encompassing a sequence within the center region of human Lamin A/C (exact sequence proprietary)
Conjugate Unconjugated
Form Liquid
Concentration 0.16 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol, 1% BSA
Contains 0.025% ProClin 300
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2736077

Product Specific Information

  • Positive Control: HeLa, A431, NIH-3T3, K562
  • Predicted Reactivity: Xenopus laevis (81%), Dog (98%), Pig (98%), Rhesus Monkey (99%), Chimpanzee (100%), Bovine (98%)
  • 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. Lamins A and C are alternatively spliced forms of the LMNA gene.
Mutations in LMNA are associated with various 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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