
Thermo Fisher Scientific Lamin A (Cleaved Asp230) Monoclonal Antibody (C.69.9)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000
Immunocytochemistry (ICC/IF)
1:100
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
C.69.9
Immunogen
Synthetic peptide corresponding to amino-terminal residues surrounding Asp230 of human lamin A if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Lamin A (Cleaved Asp230),
uniProtId:
P02545-1,
ncbiNodeId:
9606,
antigenRange:
1,
antigenLength:
664,
antigenImageFileName:
MA5-15211_Lamin_A_Cleaved_Asp230_P02545-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-15211_Lamin_A_Cleaved_Asp230_P02545-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 µg/mL
Purification
Affinity chromatography
Storage buffer
0.01M HEPES, pH 7.5, with 0.15M NaCl, 100µg/mL BSA, 50% glycerol
Contains
<0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice
RRID
AB_10985208
Product Specific Information
It is not recommended to aliquot this antibody.
This antibody is not cross-reactive with full length lamin A or C.
Target Information
The 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. Through alternate splicing, this gene encodes three type A lamin isoforms. 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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