ARVC rabbit pAb

ARVC rabbit pAb

AO-06-ES18243-100

ARVC rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES18243
Product nameARVC rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB
Other nameArmadillo repeat protein deleted in velo-cardio-facial syndrome
Size100μL
Unit price ($)248
Human gene ID421
Human Swiss-ProtO00192
SourceRabbit
IsotypeIgG
TargetARVC
Fields
Gene nameARVCF
Protein nameARVC
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID11877
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP98203
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human ARVC AA range: 563-613
SpecificityThis antibody detects endogenous levels of ARVC at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.257% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)105kD
BackgroundArmadillo Repeat gene deleted in Velo-Cardio-Facial syndrome (ARVCF) is a member of the catenin family. This family plays an important role in the formation of adherens junction complexes, which are thought to facilitate communication between the inside and outside environments of a cell. The ARVCF gene was isolated in the search for the genetic defect responsible for the autosomal dominant Velo-Cardio-Facial syndrome (VCFS), a relatively common human disorder with phenotypic features including cleft palate, conotruncal heart defects and facial dysmorphology. The ARVCF gene encodes a protein containing two motifs, a coiled coil domain in the N-terminus and a 10 armadillo repeat sequence in the midregion. Since these sequences can facilitate protein-protein interactions ARVCF is thought to function in a protein complex. In addition, ARVCF contains a predicted nuclear-targeting sequence suggesting that it may have a function as a nuclear protein. [provided by RefSeq, Jun 2010],
Functiondisease:Gene deleted in velo-cardio-facial syndrome (VCFS); it is hemizygous in all VCFS patients with interstitial deletions. This hemizygosity may play a role in the etiology of some of the phenotypes associated with VCFS characterized by a wide spectrum phenotypes, including conotruncal heart defects, cleft palate and facial dysmorphology.,function:Involved in protein-protein interactions at adherens junctions.,similarity:Belongs to the beta-catenin family.,similarity:Contains 10 ARM repeats.,tissue specificity:Found in all the examined tissues including heart, brain, liver and kidney. Found at low level in lung.,
Subcellular locationCell junction .
ExpressionFound in all the examined tissues including heart, brain, liver and kidney. Found at low level in lung. Expressed in dermal connective tissue, salivary gland duct and in the corneal layer (at protein level) (PubMed:30479852). Expressed in arrector pili muscle (at protein level) (PubMed:29034528).

Additional Images

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Western blot analysis of lysates from 293T cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES18243-100
: 10 Items
Hurry! only 10 items left in stock.

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