产品名称
Anti-Lamin A antibody produced in rabbit, affinity isolated antibody
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen 74 kDa
species reactivity
mouse, human, rat
concentration
~1 mg/mL
technique(s)
ELISA: 1:1000
immunofluorescence: 1:100-1:500
immunohistochemistry: 1:50-1:100
western blot: 1:500-1:1000
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... LMNA(4000)
Application
Anti-Lamin A antibody produced in rabbit has been used in immunoblotting.
Biochem/physiol Actions
Lamin A/C (LMNA) is involved in the structural organization of the nucleus. It modulates gene expression. It may play a role in osteoblastogenesis. Mutation in the LMNA gene is associated with muscle dystrophies, cardiomyopathies, lipodystrophies, and neuropathies. LMNA protein plays a vital role in cell cycle progression. It controls extracellular signal-regulated kinase (ERK)/mitogen-activated protein kinase (MAPK) and Wnt β-catenin pathway.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Features and Benefits
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
General description
Lamin A/C (LMNA) gene codes for lamin A and C. Lamin A/C is a nuclear intermediate filament protein. LMNA gene is mapped to human chromosome 1q22. Anti-Lamin A Antibody detects endogenous levels of total Lamin A protein.
Immunogen
The antiserum was produced against synthesized peptide derived from human Lamin A/C.
Immunogen Range: 361-410
Immunogen Range: 361-410
Physical form
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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存储类别
10 - Combustible liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
此项目有
Halida P Widyastuti et al.
BMC medical genetics, 21(1), 152-152 (2020-07-24)
Intermediate filament proteins that construct the nuclear lamina of a cell include the Lamin A/C proteins encoded by the LMNA gene, and are implicated in fundamental processes such as nuclear structure, gene expression, and signal transduction. LMNA mutations predominantly affect
Anna Sowińska-Seidler et al.
Journal of applied genetics, 59(3), 281-289 (2018-05-31)
Craniosynostosis (CS) refers to the group of craniofacial malformations characterized by the premature closure of one or more cranial sutures. The disorder is clinically and genetically heterogeneous and occurs usually as an isolated trait, but can also be syndromic. In
Hin Chu et al.
The Journal of biological chemistry, 293(30), 11709-11726 (2018-06-12)
Coronavirus tropism is predominantly determined by the interaction between coronavirus spikes and the host receptors. In this regard, coronaviruses have evolved a complicated receptor-recognition system through their spike proteins. Spikes from highly related coronaviruses can recognize distinct receptors, whereas spikes
Lorenzo Bazzani et al.
Oncotarget, 9(19), 14939-14958 (2018-03-31)
Prostaglandin E2 (PGE2) contributes to tumor progression by promoting cancer cell growth, invasion and by creating a favorable pro-tumor microenvironment. PGE2 has been reported to transactivate and internalize into the nucleus receptor tyrosine kinases such as Epidermal growth factor receptor
Elena V Ignatieva et al.
Genes, 11(9) (2020-09-11)
Laminopathies are a family of monogenic multi-system diseases resulting from mutations in the LMNA gene which include a wide range of neuromuscular disorders. Although lamins are expressed in most types of differentiated cells, LMNA mutations selectively affect only specific tissues
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