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Anti-Filamin A Rabbit mAb [28R89L14]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R014708
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-Filamin A Rabbit mAb [28R89L14]
Anti-Filamin A Rabbit mAb [28R89L14]
Product NameAnti-Filamin A Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IF (Cell)/ICC, ELISA
DilutionWB 1:1,000~1:6,000; IF 1:100~1:200
ReactivityHuman, Mouse, Rat
HostRabbit
ClonalityMonoclonal
Clone No.28R89L14
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human Filamin A
FormatAffinity purified monoclonal antibody supplied in PBS with 0.01% sodium azide and 50% glycerol, pH 7.3.
SynonymsABP 280, ABP-280, Actin-binding protein 280, Alpha filamin, Alpha-filamin, APBX, CSBS, CVD1, Endothelial actin binding protein, Endothelial actin-binding protein, Filamin 1, Filamin A alpha, Filamin A, Filamin-1, Filamin-A, FLN, FLN-A, FLN1, FLNA, FLNA_HUMAN, FMD, MNS, NHBP, Non muscle filamin, Non-muscle filamin, OPD, OPD1, OPD2, XLVD, XMVD.
Molecular weightCalculated MW: 281 kDa; Observed MW: 281 kDa
Uniprot ID P21333
Gene ID 2316
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-Filamin A Rabbit mAb [28R89L14] is for research use only and not for use in diagnostic or therapeutic procedures.
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]
Cellular Location Cytoplasm > cell cortex. Cytoplasm > cytoskeleton.
Tissue Location Ubiquitous.

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