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Lamin A/C Recombinant Rabbit mAb (PE Conjugate) (SDT-R041)

Lamin A/C Recombinant Rabbit mAb (PE Conjugate) (SDT-R041)

Catalog Number: S0B6217 Application: ICFCM Reactivity: Human Conjugation: PE Brand: Starter
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Regular price $45 USD
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Product Details

Product Specification


Host Rabbit
Antigen Lamin A/C
Synonyms Prelamin-A/C, 70 kDa lamin, Renal carcinoma antigen NY-REN-32
Accession P02545
Clone Number SDT-R041
Antibody Type Recombinant mAb
Isotype IgG
Application ICFCM
Reactivity Hu
Positive Sample HeLa
Purification Protein A
Concentration 1 mg/ml
Conjugation PE
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
ICFCM 1:1000 Hu

Background

Lamins are a class of intermediate filament proteins that form a matrix on the inner surface of the nuclear envelope. These proteins are found in many different cell types in three different forms (A, B, and C). Lamins A and C are alternatively spliced versions of the LMNA gene. Lamin A has a mass of about 74kDa while Lamin C is 65kDa. Mutations in the LMNA gene are associated with several serious human diseases, including Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease type 2B1, and Hutchinson-Gilford progeria syndrome.

Picture

FC

Flow cytometric analysis of Lamin A/C expression on 4% PFA fixed 90% methanol permeabilized HeLa cells. Cells from the HeLa (Human cervix adenocarcinoma epithelial cell) or Jurkat (Human T cell leukemia T lymphocyte, Left) was stained with Phycoerythrin Rabbit IgG Isotype Control (Black line histogram) or SDT Lamin A/C Recombinant Rabbit mAb (Alexa Fluor® 488 Conjugate) Lamin A/C Recombinant Rabbit mAb (PE Conjugate) (Red line histogram) at 1/1000 dilution (0.1 μg), cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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