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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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Rabbit에서 생산된 Lamin A+C에 대한 Polyclonal Antibody로, Western blot 및 Flow cytometry에 적합합니다. KLH-결합 합성 펩타이드(400-450 aa, human Lamin A)를 면역원으로 사용하였으며, 핵 라미나 구조 연구 및 Lamin 관련 질환 연구에 활용 가능합니다.

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Thermo Fisher Scientific A0145540 Lamin A+C Polyclonal Antibody 40 ug pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A+C Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 0.5–1 µg/mL –
Flow Cytometry (Flow) 1–3 µg / 1×10⁶ cells –
Miscellaneous PubMed (Misc) – View 5 publications

Product Specifications

Specification Description
Published species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH-coupled synthetic peptide within residues 400–450 of human Lamin A (Swiss Prot: P02545)
Conjugate Unconjugated
Form Lyophilized
Storage conditions −20°C or −80°C if preferred
Shipping conditions Wet ice

Product Specific Information

Reconstitute the lyophilized powder with deionized water (or equivalent) to a final concentration of 0.5 mg/mL.

Lamins are structural protein components of the nuclear lamina, which contains three members: Lamin A, B, and C in mammalian cells. Lamin A and Lamin C are generated by alternative splicing from the same gene and share complete identity for the first 566 amino acids. Lamin A interacts with transcription factor SREBP1 via its C-terminal domain. Lamin A/C deficiency is associated with defective nuclear mechanics and impaired transcriptional activation. Lamin A/C is cleaved by caspase-6 and serves as a marker for caspase-6 activation.

This antibody (Rabbit Anti-Lamin A+C Polyclonal Antibody) is developed in rabbit using a KLH-coupled synthetic peptide within residues 400–450 of human Lamin A (Swiss Prot: P02545).


Target Information

Lamins are intermediate filament proteins that form a matrix on the inner surface of the nuclear envelope. These proteins exist in multiple cell types as three major forms (A, B, and C). Lamins A and C are alternatively spliced products of the LMNA gene.

Mutations in the LMNA gene 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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