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Lamin A/C Antibody

CAT: 0013-GTR18304582Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18304582Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
A synthetic peptide of human Lamin A/C
Product Name Alternative
LMNA; LMN1; Prelamin-A/C
UniProt
P02545
Reactivity
Human, Mouse, Rat
Immunogen
A synthetic peptide of human Lamin A/C
Target
Disease
Clonality
Monoclonal
Conjugation
Unconjugated
Concentration
Approximately 1mg/ml (varies from batch to batch) . Please inquire for precise concentration.
Dilution
WB: 1/500-1/1000; IP: 1212122025120; IHC: 1/50-1/100; IF/ICC: 1/50-1/200
Molecular Weight
Calculated MW: 74 kDa; Observed MW: 74,63 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ICC, IHC, IP, WB
Host or Source
Rabbit
Preservative
Purified antibody in TBS with 0.05% sodium azide,0.05%rAlbumin and 50% glycerol.
Isotype
Rabbit IgG
Entrez
4000

UniProtKB · P02545

Prelamin-A/C

LMNA_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P02545
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
LMNA
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
B4DI32, D3DVB0, D6RAQ3, E7EUI9, P02546, Q5I6Y4, Q5I6Y6, Q5TCJ2, Q5TCJ3, Q6UYC3, Q969I8, Q96JA2
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationGlycoproteinIsopeptide bondLipoproteinMethylationPhosphoproteinPrenylationUbl conjugation

Coding sequence diversity

Alternative splicing

Disease

CardiomyopathyCharcot-Marie-Tooth diseaseCongenital muscular dystrophyDisease variantEmery-Dreifuss muscular dystrophyLimb-girdle muscular dystrophyNeurodegenerationNeuropathy

Domain

Coiled coil

Cellular component

Intermediate filamentNucleus

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