Lamin A/C Monoclonal Antibody (4C4) | Invitrogen MA5-47328 product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Invitrogen

other brands :

NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience

product type :

antibody

product name :

Lamin A/C Monoclonal Antibody (4C4)

catalog :

MA5-47328

quantity :

500 uL

price :

US 1648.00

clonality :

monoclonal

host :

mouse

conjugate :

nonconjugated

clone name :

4C4

The same clone is also sold as:

Abcam: ab190380
Novus Biologicals: NBP2-25151
Rockland Immunochemicals: 200-301-X12

reactivity :

human, rat

application :

western blot, immunocytochemistry

product information

Product Type :

Antibody

Product Name :

Lamin A/C Monoclonal Antibody (4C4)

Catalog # :

MA5-47328

Quantity :

500 uL

Price :

US 1648.00

Clonality :

Monoclonal

Purity :

Protein A/G

Host :

Mouse

Reactivity :

Human, Rat

Applications :

Immunocytochemistry: 1:1,000, Western Blot: 1:1,000-1:2,000

Species :

Human, Rat

Clone :

4C4

Isotype :

IgG1

Storage :

Store at 4 C short term. For long term storage, store at -20 C, avoiding freeze/thaw cycles.

Description :

Lamins are a class of intermediate filament proteins that form a matrix on the inner surface of the nuclear envelope. These proteins are found in many different cell types in three different forms (A, B, and C). Lamins A and C are alternatively spliced versions of the LMNA gene. The LMNA gene has been linked to many disorders of the muscular system, nervous system, and the fat distributions systems including: Emery-Dreifuss muscular dystrophy, Dunnigan-type familial partial lipodystrophy (FPLD), limb-girdle muscular dystrophy (LGMD1B), dilated cardiomyopathy (CMD1A), axonal neuropathy (Charcot-Marie-Tooth disease; CMT2B1), and mandibuloacral dysplasia (MAD).

Immunogen :

Full length recombinant human lamin A expressed in and purified from E. coli.

Format :

Liquid

Applications w/Dilutions :

Immunocytochemistry: 1:1,000, Western Blot: 1:1,000-1:2,000

Aliases :

70 kDa lamin; cb948; CDCD1; CDDC; CMD1A; CMT2B1; Dhe; EMD2; FPL; FPLD; FPLD2; HGPS; I79_009616; IDC; lamin; lamin A; lamin A/C; lamin A/C L homeolog; lamin A/C-like 1; Lamin A+C mutant; Lamin AC; lamin a-c; lamin C; lamin C2; lamin-A; Lamin-A/C; LDP1; LFP; LGMD1B; LMN1; lmna; LMNA protein; lmna.L; lmna-A; LMNC; LMNL1; mutant 453W; Mutant lamin A/C; nuclear intermediate filament protein; nuclear lamin A; prelamin-A/C; PRO1; progerin mutant; Renal carcinoma antigen NY-REN-32; RP11-54H19.1; unnamed protein product; wu:fk66d12; XELAEV_18040808mg