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Lamin A/C Antibody

CAT: 0013-GTR18793169Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18793169Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Our Anti-Lamin A/C mouse monoclonal primary antibody detects human Lamin A/C, and is IgG. It is validated for use in FC, ICC, WB.
UniProt
P02545
Reactivity
Human
Immunogen
Full length recombinant human Lamin C
Target
Lamin A/C
Clonality
Monoclonal
Clone
4C4
Conjugation
Unconjugated
Dilution
WB: 1:1000-1:2000; ICC: 1:500-1:1000
Form
Lyophilized
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.
Applications Notes
Use 2 ug/10^6 cells for Flow cytometry.
Tested Applications
FC, ICC, WB
Host or Source
Mouse
Preservative
Lyophilized from PBS buffer pH 7.2-7.6 with 5% trehalose, and sodium azide
Isotype
IgG1

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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