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Western blot analysis of extracts of various cell lines, using Filamin A Rabbit mAb (A3738) at 1:1000 dilution.|Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.|Lysates/proteins: 25ug per lane.|Blocking buffer: 3% nonfat dry milk in TBST.|Detection: ECL Basic Kit (RM00020).|Exposure time: 1s.
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Immunohistochemistry of paraffin-embedded rat ovary using Filamin A Rabbit mAb (A3738) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded human colon using Filamin A Rabbit mAb (A3738) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded mouse kidney using Filamin A Rabbit mAb (A3738) at dilution of 1:100 (40x lens).
Filamin A Rabbit mAb
Catalog No：AB-A3738
Manufacturer：ABclonal
Synonyms：ABP-280, ABPX, CSBS, CVD1, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD
Applications：WB,IHC
Reactivity：Human,Mouse,Rat
Host：Rabbit
Conjugate：No
€65,00 – €485,00
| Product Name: | Filamin A Rabbit mAb |
| Category: | Monoclonal Antibodies |
| Description: | 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] |
| Immunogen: | A synthesized peptide derived from human Filamin A |
| Gene ID: | 2316 |
| Swiss prot: | P21333 |
| Molecular weight: | 281kDa |
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