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Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (131C3)
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Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (131C3)

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Lamin A/C 단백질을 인식하는 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (Clone 131C3). Western blot, IHC, ICC/IF, Flow cytometry 등 다양한 응용 가능. Human, Mouse 등 여러 종에 반응하며 1 mg/mL 농도의 액상형 비접합 항체. 연구용으로만 사용.

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Thermo Fisher Scientific MA106102 Lamin A/C Monoclonal Antibody (131C3) 100 ug pk판매 단위 pk
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698,000원VAT 포함 767,800원

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (131C3)

Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (131C3)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:100–1:1,000 View 1 publication
Immunohistochemistry (Frozen) (IHC (F)) 1:100–1:200 View 1 publication
Immunocytochemistry (ICC/IF) Assay-dependent View 1 publication
Flow Cytometry (Flow) 1:100–1:200 View 1 publication
Miscellaneous PubMed (Misc) - View 1 publication

Product Specifications

Specification Description
Species Reactivity Bovine, Dog, Hamster, Human, Mouse, Sheep, Rat
Published Species Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone 131C3
Immunogen Purified rat liver lamin
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Purified
Storage Buffer PBS
Contains 0.09% sodium azide
Storage Conditions Store at 4°C short term; for long term, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_559890

Product Specific Information

  • MA1-06102 detects lamin A and C in human, mouse, rat, bovine, hamster, sheep, and canine samples.
  • Successfully used in immunocytochemistry, immunohistochemistry, FACS, and Western blotting procedures.
  • Immunogen: purified rat liver lamins.
  • Reacts with an epitope located between residues 319–566 in lamin A and C.

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 versions of the LMNA gene.
Mutations in LMNA are associated with various disorders such as:

  • 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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