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Rabbit Recombinant Monoclonal Lamin B1 antibody - conjugated to Alexa Fluor® 750.

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Key facts

Isotype
IgG
Host species
Rabbit
Conjugation
Alexa Fluor® 750
Excitation/Emission
Ex: 749nm, Em: 775nm
Storage buffer

pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 68% PBS, 30% Glycerol (glycerin, glycerine), 1% BSA

Form
Liquid
Clonality
Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Application
Target Binding Affinity
Reactivity
Expected
Dilution info
-
Notes

-

Application
Antibody Labelling
Reactivity
Expected
Dilution info
-
Notes

-

Target data

Function

Lamins are intermediate filament proteins that assemble into a filamentous meshwork, and which constitute the major components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane (PubMed:28716252, PubMed:32910914). Lamins provide a framework for the nuclear envelope, bridging the nuclear envelope and chromatin, thereby playing an important role in nuclear assembly, chromatin organization, nuclear membrane and telomere dynamics (PubMed:28716252, PubMed:32910914). The structural integrity of the lamina is strictly controlled by the cell cycle, as seen by the disintegration and formation of the nuclear envelope in prophase and telophase, respectively (PubMed:28716252, PubMed:32910914).

Additional Targets

LMNA, LMNA

Alternative names

Recommended products

Rabbit Recombinant Monoclonal Lamin B1 antibody - conjugated to Alexa Fluor® 750.

Key facts

Isotype
IgG
Conjugation
Alexa Fluor® 750
Excitation/Emission
Ex: 749nm, Em: 775nm
Form
Liquid
Clonality
Monoclonal
Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Clone number
EPR4068
Purification technique
Affinity purification Protein A
Specificity

The antibody recognizes full length Lamin A/B1/C and the cleaved small unit.

Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle, Store in the dark

Notes

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

How are conjugated primary antibodies validated?
This conjugated primary antibody is released using a quantitative quality control method that evaluates binding affinity post-conjugation and efficiency of antibody labeling.
For suitable applications and species reactivity, please refer to the unconjugated version of this clone.

Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

Lamin A Lamin B1 and Lamin C are nuclear envelope proteins critical for nuclear structure and stability. Lamin A and Lamin C both originating from the LMNA gene have molecular masses of about 74 kDa and 65 kDa respectively due to alternative splicing. Lamin B1 encoded by the LMNB1 gene has a molecular mass of around 67 kDa. These lamins are found in the nuclear lamina a dense fibrillar network lining the inner surface of the nuclear envelope. They anchor chromatin to the nuclear envelope and play roles in DNA replication repair and gene expression.

Biological function summary

Lamins play essential roles in maintaining cell integrity and regulating gene expression. Lamin A and Lamin C part of the type A lamins and Lamin B1 part of the type B lamins contribute to nuclear organization and mechanical support. These proteins form complexes within the lamina network and with other nuclear proteins participating in chromatin organization and gene transcription. Defects in lamins negatively impact cellular functions and can lead to altered gene expression patterns.

Pathways

Lamins interact with multiple signaling pathways that govern cellular homeostasis and stress response. They play roles in the mechanotransduction pathway influencing how cells perceive mechanical stress and respond to it. Interaction with proteins like emerin and nuclear actin further connects lamins to pathways involved in gene regulation and structural support of the nucleus.

Associated diseases and disorders

Lamin dysfunction has associations with several human diseases including laminopathies such as Hutchinson-Gilford progeria syndrome and muscular dystrophy. Mutations in the LMNA gene affecting Lamin A and Lamin C often lead to disrupted nuclear architecture and impaired cellular function. Lamin B1 when overexpressed or mutated has links to neurological disorders like autosomal dominant leukodystrophy. These associations highlight the importance of lamins in disease mechanisms and provide insights into potential therapeutic targets.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

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    Product protocols

    For this product, it's our understanding that no specific protocols are required. You can:

    Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

    For licensing inquiries, please contact partnerships@abcam.com