CD2AP Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5114714-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5114714 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
CD2AP
Classification
Polyclonal
Conjugate
Unconjugated
Gene
CD2AP
Gene Alias
adapter protein CMS; AL024079; C78928; Cas ligand with multiple SH3 domains; Cas ligand with multiple Src homology 3 (SH3) domains; CD2 associated protein; Cd2ap; CD2-associated protein; CMS; mesenchyme to epithelium transition protein, SH3 domains; mesenchyme-to-epithelium transition protein with SH3 domains 1; Mets1; METS-1; SH3 domain-containing adapter protein; SH3 domain-containing adaptor protein METS-1
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
12488, 23607, 316258
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide
Gene Accession No.
F1LRS8, Q9JLQ0, Q9Y5K6
Gene Symbols
CD2AP
Immunogen
A synthesized peptide derived from human CD2AP(Accession Q9Y5K6), corresponding to amino acid residues T188-E238.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total CD2AP
- This gene encodes a scaffolding molecule that regulates the actin cytoskeleton
- The protein directly interacts with filamentous actin and a variety of cell membrane proteins through multiple actin binding sites, SH3 domains, and a proline-rich region containing binding sites for SH3 domains
- The cytoplasmic protein localizes to membrane ruffles, lipid rafts, and the leading edges of cells
- It is implicated in dynamic actin remodeling and membrane trafficking that occurs during receptor endocytosis and cytokinesis
- Haploinsufficiency of this gene is implicated in susceptibility to glomerular disease.