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Progerin Monoclonal Antibody (13A4), Active Motif™
SDP

Catalog No. 501993008
Encompass
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50-199-3008 10 μg
50-199-3007 100 μg
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Catalog No. 50-199-3008 Supplier Active Motif Supplier No. 39966
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Mouse Monoclonal Antibody

Progerin is a 614 amino acid protein involved in Hutchinson-Gilford progeria syndrome. Progerin is most often generated by a point mutation (C1824T) in the LMNA gene that codes for lamin-A/C. This mutation activates a cryptic splice site and gives rise to a form of lamin A with a 50-amino acid internal deletion within the C-terminal domain of the protein. Approximately 80% of Hutchinson-Gilford progeria syndrome cases carry a single copy of the most common mutation, a silent point mutation, G608G (GGC > GGT), within exon 11 of the LMNA gene.

Specifications

Antigen Progerin
Applications Immunocytochemistry, Immunofluorescence, Western Blot
Classification Monoclonal
Clone 13A4
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation 70mM tris with 0.07mM EDTA, 105mM NaCl, 30% glycerol, 31mM glycine and 0.035% sodium azide; pH 8
Gene LMNA
Gene Accession No. P02545
Gene Alias 70 kDa lamin; CDCD1; CDDC; CMD1A; CMT2B1; EMD2; FPL; FPLD; FPLD2; HGPS; IDC; lamin; lamin A/C; lamin A/C-like 1; Lamin AC; Lamin-A/C; LDP1; LFP; LGMD1B; LMN1; LMNA; LMNC; LMNL1; Mutant lamin A/C; Prelamin-A/C; PRO1; progerin mutant; Renal carcinoma antigen NY-REN-32
Gene Symbols LMNA
Host Species Mouse
Immunogen This Progerin antibody was raised against a peptide corresponding to amino acids 604-611 of human Progerin.
Purification Method Protein G
Quantity 10 μg
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 4000
Target Species Human
Content And Storage -20°C, Avoid Freeze/Thaw Cycles
Product Type Antibody
Form Liquid
Isotype IgG1 κ
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