LFTY2 rabbit pAb

LFTY2 rabbit pAb

AO-06-ES15164-100

LFTY2 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES15164
Product nameLFTY2 rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB
Other name
Size100μL
Unit price ($)248
Human gene ID7044
Human Swiss-ProtO00292
SourceRabbit
IsotypeIgG
TargetLFTY2
Fields>>TGF-beta signaling pathway;>>Signaling pathways regulating pluripotency of stem cells
Gene nameLEFTY2 EBAF LEFTA LEFTYA TGFB4 PSEC0024
Protein nameLFTY2
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID320202
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP57785
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human LFTY2 AA range: 205-255
SpecificityThis antibody detects endogenous levels of LFTY2 at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% 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)40kD
Observed band (KD)
BackgroundThis gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which plays a role in left-right asymmetry determination of organ systems during development. The protein may also play a role in endometrial bleeding. Mutations in this gene have been associated with left-right axis malformations, particularly in the heart and lungs. Some types of infertility have been associated with dysregulated expression of this gene in the endometrium. This gene is closely linked to both a related family member and a related pseudogene. This gene encodes multiple isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016],
Functiondevelopmental stage:Transiently expressed before and during menstrual bleeding.,disease:Defects in LEFTY2 are the cause of left-right axis malformations (L-R axis malformation) [MIM:601877]. The defect includes left pulmonary isomerism, with cardiac anomalies characterized by complete atrioventricular canal defect and hypoplastic left ventricle, and interrupted inferior vena cava.,function:Required for left-right (L-R) asymmetry determination of organ systems in mammals. May play a role in endometrial bleeding.,PTM:The processing of the protein may also occur at the second R-X-X-R site located at AA 132-135. Processing appears to be regulated in a cell-type specific manner.,sequence caution:Authors have revised their sequence, but have not submitted the revised DNA sequence.,similarity:Belongs to the TGF-beta family.,tissue specificity:Mesenchymal cells of the endometrial stroma.,
Subcellular locationSecreted.
ExpressionMesenchymal cells of the endometrial stroma.

Additional Images

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Western blot analysis of lysates from HpeG2 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES15164-100
: 10 Items
Hurry! only 10 items left in stock.

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