Phospho-Filamin A/B (Ser2152/Ser2107) Rabbit pAb
Cat#:DPA05443应用:WB,IHC,ICC/IF
Product Name: | Phospho-Filamin A/B (Ser2152/Ser2107) Recombinant Rabbit mAb |
Cat No.: | RMA03040 |
Clonality: | Monoclonal |
Species Reactivity: | Human |
Tested Applications: | WB,IHC,ICC/IF |
Recommended Dilution: | WB: 1:1000-1:5000 IHC: 1:20 ICC/IF: 1:50 |
Size: | 30ul 50ul 100uL |
Format: | Liquid |
Source: | Rabbit |
Purification Method: | Affinity Purification |
Isotype: | IgG |
Conjugate: | Un-conjugated |
Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
Immunogen: | A synthetic phosphopeptide corresponding to residues surrounding Ser2152 of human Filamin A |
Calculated Molecular Weight: | 281 kDa |
Observed Molecular Weight: | 281 kDa |
GenBank Accession Number: | O75369 |
Gene ID (NCBI): | 2316 |
Synonyms: | FLN; FMD; MNS; OPD; ABPX; CSBS; CVD1; FGS2; FLN1; NHBP; OPD1; OPD2; XLVD; XMVD; FLN-A; ABP-280 |
Background: | The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009] |
Category: | Primary Ab |