Mouse Monoclonal Anti-Lamin B1 antibody (STJ99312)


Reactivity: Human, Mouse, Monkey
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal Anti-Lamin B1 antibody (STJ99312)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, ELISA

Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|ADLD antibody|CMD1A antibody|CMT2B1 antibody|Lamin A/C antibody|Lamin B1 antibody|Lamin B2 antibody|LMN2 antibody|LMNA antibody|LMNB1 antibody|LMNB2 antibody|Anti-Lamin B1 antibody – Nuclear Envelope Marker (ab16048)
SCBT cat No: sc-6216|sc-6217|sc-160482|sc-56143|sc-56144|sc-377000|sc-374015|sc-365214|sc-365962|sc-377001|sc-373918|sc-20682|sc-30264|


Anti-Lamin B1 antibody

Catalogue No.



Human, Mouse, Monkey


Anti-Lamin B1 antibody detects endogenous levels of Lamin B1 and does not cross-react with related proteins.


Recombinant human Lamin B1 protein.











Molecular weight



Anti-Lamin B1 antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.


1 mg/ml


Anti-Lamin B1 antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.


-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

ADLD antibody, CMD1A antibody, CMT2B1 antibody, Lamin A/C antibody, Lamin B1 antibody, Lamin B2 antibody, LMN2 antibody, LMNA antibody, LMNB1 antibody, LMNB2 antibody

Protein function

Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin.

Involvement in disease

Leukodystrophy, demyelinating, autosomal dominant, adult-onset (ADLD) [MIM:169500]: A slowly progressive and fatal demyelinating leukodystrophy, presenting in the fourth or fifth decade of life. Clinically characterized by early autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS. It differs from multiple sclerosis and other demyelinating disorders in that neuropathology shows preservation of oligodendroglia in the presence of subtotal demyelination and lack of astrogliosis. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the intermediate filament family. ; Contains 1 LTD domain.

Protein post-translational modifications

B-type lamins undergo a series of modifications, such as farnesylation and phosphorylation. Increased phosphorylation of the lamins occurs before envelope disintegration and probably plays a role in regulating lamin associations.

Protein cellular localization

Nucleus inner membrane; Lipid-anchor; Nucleoplasmic side.

Research area

<a href="">All research areas</a>><a href="">Tumor Suppressor/Apoptosis</a>><a href="">Lamin</a><br><a href=""&gt; (View all antibody categories related to Tumor Suppressor/Apoptosis)</a>


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St John’s Laboratory Ltd.

Product type

Primary antibody


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