
Thermo Fisher Scientific Lamin A Monoclonal Antibody (133A2)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:100-1:1,000
View 2 publications 2 publications
Immunohistochemistry (Paraffin) (IHC (P))
1:100-1:200
Immunohistochemistry (Frozen) (IHC (F))
1:100-1:200
Immunocytochemistry (ICC/IF)
1:100-1:200
View 3 publications 3 publications
Flow Cytometry (Flow)
1:100-1:200
Product Specifications
Species Reactivity
Bovine, Dog, Human, Mouse, Rat
Published species
Human
Host/Isotype
Mouse / IgG3
Class
Monoclonal
Type
Antibody
Clone
133A2
Immunogen
Partially purified recombinant human lamin A. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Lamin A,
uniProtId:
P02545-1,
ncbiNodeId:
9606,
antigenRange:
1-664,
antigenLength:
664,
antigenImageFileName:
MA1-06101_Lamin_A_P02545-1_House_mouse.svg,
antigenImageFileNamePDP:
MA1-06101_Lamin_A_P02545-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Ion-exchange chromatography
Storage buffer
PBS
Contains
0.09% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_559889
Product Specific Information
MA1-06101 detects lamin A in human, mouse, rat, bovine and canine samples.
MA1-06101 has sucessfully been used in immunocytochemistry, immunohistochemistry (paraffin), flow cytometry, and Western blotting procedures.
The MA1-06101 immunogen is partially purified recombinant human lamin A.
Target Information
Nuclear lamins form a network of intermediate-type filaments at the nucleoplasmic site of the nuclear membrane. Two main subtypes of nuclear lamins can be distinguished, i.e. A-type lamins and B-type lamins. The A-type lamins comprise a set of three proteins arising from the same gene by alternative splicing, i.e. lamin A, lamin C and lamin Adel 10, while the B-type lamins include two proteins arising from two distinct genes, i.e. lamin B1 and lamin B2. Recent evidence has revealed that mutations in A-type lamins give rise to a range of rare but dominant genetic disorders, including Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy with conduction-system disease and Dunnigan-type familial partial lipodystrophy. In addition, the expression of A-type lamins coincides with cell differentiation and as A-type lamins specifically interact with chromatin, a role in the regulation of differential gene expression has been suggested for A-type lamins.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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