KD-Validated FLNA Recombinant Rabbit Monoclonal Antibody

KD-Validated FLNA Recombinant Rabbit Monoclonal Antibody

Cat. No.: KVAb01615
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,IHC-P

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Gene Name:FLNA
Category: KO&KD Validated Antibodies Tags: , , , , , , , , ,

Summary

Production Name

KD-Validated FLNA Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,IHC-P

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

FLNA

Alternative Names

FLNA; Filamin A; ABP-280; FLN1; FLN; Endothelial Actin-Binding Protein; Actin Binding Protein 280; Non-Muscle Filamin; Filamin A, Alpha; Alpha-Filamin; Filamin-A; Filamin-1; FLN-A; OPD1; OPD2; Filamin A, Alpha (Actin Binding Protein 280); Epididymis Secretory Sperm Binding Protein; Actin-Binding Protein 280; Alpha Filamin; EC 2.1.1.43; EC 6.3.4.4; ABPX; CSBS; CVD1; FGS2; NHBP; XLVD; XMVD; FMD; MNS; OPD

Gene ID

2316

SwissProt ID

P21333

 

Application

Dilution Ratio

WB 1:2,000-1:10,000; FC 1:200-1:2,000; IHC-P 1:100-1:200

Molecular Weight

Calculated MW: 280.7kDa

 

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]

 

Research Area

Signal Transduction,Neuroscience

   💬 WhatsApp