Lamin B2 Monoclonal Antibody (GT144), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA517274-Each-of-1 | In Stock | ₹ 47,036.50 |
PIMA517274 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,036.50
GST (18%): ₹ 8,466.57
Total Price: ₹ 55,503.07
Antigen
Lamin B2
Classification
Monoclonal
Concentration
0.81 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
Q03252
Gene Symbols
LMNB2
Immunogen
Recombinant fragment contains a sequence corresponding to a region within amino acids 277 and 600 of Lamin B2
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG2a
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot
Clone
GT144
Conjugate
Unconjugated
Gene
LMNB2
Gene Alias
EPM9; fc15d06; im:7142331; LAMB2; lamin; lamin A/C; lamin B2; lamin B2 S homeolog; lamin B3; lamin-B2; Lamin-L(II); LMN2; LMNA; lmnb2; lmnb2.S; lmnb2-a; lmnb2-b; MGC2721; RGD1563803; unnamed protein product; wu:fb94e05; wu:fb95e12; wu:fc15d06; wu:fc49h03; XELAEV_18009631mg
Host Species
Mouse
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
84823
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Related Products
Description
- Recommended positive controls: U87-MG, SK-N-SH, IMR32, SK-N-AS, HepG2, HepG2 nuclear
- Predicted reactivity: Bovine (83%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- 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.