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Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (mab636)
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Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (mab636)

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Lamin A/C 단백질을 인식하는 Thermo Fisher monoclonal antibody (mab636). Western blot, IHC, ICC/IF 등 다양한 응용에 사용 가능. 인간, 소, 돼지 등에서 반응하며, Protein A 정제 및 PBS/BSA buffer에 보관. 연구용으로만 사용.

카탈로그번호
MA31000
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 06:14
Thermo Fisher Scientific MA31000 Lamin A/C Monoclonal Antibody (mab636) 200 ul pk판매 단위 pk ·
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525,000원VAT 포함 577,500원

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Monoclonal Antibody (mab636)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:100–1:2,000 View 15 publications
Immunohistochemistry (IHC) View 5 publications
Immunohistochemistry (Frozen) (IHC (F)) 1:100
Immunocytochemistry (ICC/IF) 1:100 View 11 publications
Flow Cytometry (Flow) View 1 publication

Product Specifications

Specification Description
Species Reactivity Bovine, Human, Pig
Published Species Human, Mouse, Pig
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone mab636
Immunogen Porcine lamin preparation
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_325377

Product Specific Information

MA3-1000 detects lamin A/C from human, bovine, porcine, and canine samples.
It has been successfully used in Western blot, immunofluorescence, and immunohistochemistry procedures.
By Western blot, this antibody detects approximately 70 and 65 kDa proteins corresponding to lamin A and C, respectively, from HeLa cell extract.
It is also useful for subcellular localization experiments and has been widely used for detection of lamin A/C control in siRNA experiments.
The MA3-1000 antigen is a porcine lamin preparation.


Target Information

Lamins are intermediate filament proteins forming a matrix on the inner surface of the nuclear envelope.
They exist in several forms (A, B, and C), with lamins A and C being alternatively spliced products 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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