Filensin Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA529976-Each-of-1 | In Stock | ₹ 47,392.50 |
PIPA529976 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,392.50
GST (18%): ₹ 8,530.65
Total Price: ₹ 55,923.15
Antigen
Filensin
Classification
Polyclonal
Conjugate
Unconjugated
Gene
BFSP1
Gene Alias
Beaded filament structural protein 1; beaded filament structural protein 1, filensin; BFSP1; CP115; CP94; CTRCT33; cytoskeletal protein, 115 KD; filensin; Lens fiber cell beaded-filament structural protein CP 115; lens intermediate filament-like heavy; LIFL-H; LOW QUALITY PROTEIN: filensin; RP4-531H16.2
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
631
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
Q12934
Gene Symbols
BFSP1
Immunogen
Recombinant fragment corresponding to a region within amino acids 89 and 344 of Human Filensin
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: HCT116
- Predicted reactivity: Mouse (81%), Rat (84%), Bovine (82%), Guinea pig (81%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- More than 99% of the vertebrate ocular lens is comprised of terminally differentiated lens fiber cells
- Two lens-specific intermediate filament-like proteins, CP49 (also known as phakinin) and the protein product of this gene, filensin, are expressed only after fiber cell differentiation has begun
- Both proteins are found in a structurally unique cytoskeletal element that is referred to as the beaded filament (BF)
- Mutations in this gene are the cause of autosomal recessive cortical juvenile-onset cataract
- Multiple transcript variants encoding different isoforms have been found for this gene.