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Phospho-Filamin A/B (Ser2152/Ser2107) Recombinant Rabbit mAb

Cat No.: RMA03040
规格:
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  • Western blot analysis of Anti-Phospho-Filamin A/B (Ser2152/Ser2107) antibody(RMA03040) Gel: 6%SDS-PAGE Lysate: 20 μg Primary antibody: RMA03040(Phospho-Filamin A/B (Ser2152/Ser2107) antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

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
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