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Lamin A/C (5D12) Mouse mAb

CAT: 0013-GTR18243053-01Size: 20 ulDry Ice: NoHazardous: No
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CAT#:0013-GTR18243053-01Size:20 ul
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Description
Lamin A/C (5D12) Mouse mAb
Product Name Alternative
LMNA; LMN1; Prelamin-A/C
UniProt
P02545
Reactivity
Human, Mouse, Rat
Immunogen
Purified recombinant human LMNA protein fragments expressed in E.coli.
Target
LMNA
Clonality
Monoclonal
Clone
B7F34XE8XG1
Conjugation
Unconjugated
Field of Research
Disease Biomarkers
Purification
Affinity Purified
Concentration
1 mg/ml
Dilution
WB: 1/500-1/1000 IF: 1/50-1/200
Form
Liquid
Molecular Weight
Calculated MW: 74 kDa; Observed MW: 63,74 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, IF, WB
Preservative
Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.02% sodium azide, pH 7.3.
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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