![WB analysis of 10microg nuclear extract from fractionated mouse tissue lysate using GTX80813 Lamin A + C antibody [mab636]. Dilution : 1:500 WB analysis of 10microg nuclear extract from fractionated mouse tissue lysate using GTX80813 Lamin A + C antibody [mab636]. Dilution : 1:500](https://www.genetex.com/upload/website/prouct_img/normal/GTX80813/GTX80813_1958_WB_w_23061322_879.webp)
WB analysis of 10microg nuclear extract from fractionated mouse tissue lysate using GTX80813 Lamin A + C antibody [mab636]. Dilution : 1:500
Lamin A + C antibody [mab636]
GTX80813
Overview
- SupplierGeneTex
- Product NameLamin A + C antibody [mab636]
- Delivery Days Customer9
- Application Supplier NoteWB: 1:100 - 1:2000. ICC/IF: 1:100. IHC-Fr: 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- Clone IDmab636
- FormulationLiquid
- Gene ID4000
- Target nameLMNA
- Target descriptionlamin A/C
- Target synonyms70 kDa lamin; CDCD1; CDDC; CMD1A; CMT2B1; EMD2; epididymis secretory sperm binding protein; FPL; FPLD; FPLD2; HGPS; IDC; lamin; lamin A/C-like 1; LDP1; LFP; LGMD1B; LMN1; LMNC; LMNL1; MADA; mandibuloacral dysplasia type A; prelamin-A/C; PRO1; renal carcinoma antigen NY-REN-32
- Protein IDP02545
- Protein NamePrelamin-A/C
- Scientific DescriptionThe nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, Apr 2012]
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203