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Rabbit anti-IRF6 polyclonal antibody - middle region

Catalog Number:OM105940
OM105940
Discount Price
OM105940-100ul
1~2 Week
100ul
OM105940-50ul
50ul
OM105940-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-IRF6 polyclonal antibody - middle region
Antibody Type Primary Antibodies
Antigen Alias LPS, OFC6, PIT, PPS, VWS, VWS1
Immunogen The immunogen for anti-IRF6 antibody: synthetic peptide directed towards the middle region of human IRF6
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity BovineDogHorseHumanMousePigRabbitRatSheepZebra Fish
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol IRF6
Gene Synonyms LPS
OFC6
PIT
PPS
VWS
VWS1
Gene Full Name Interferon regulatory factor 6
Gene Summary IRF6 is a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. Mutations in its gene can cause van der Woude syndrome and popliteal pterygium syndrome. This protein is involved in palate formation.The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eucaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. This protein is involved in palate formation. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alternative Names LPS
OFC6
PIT
PPS
VWS
VWS1
Molecular Weight(MW) 53kDa
Sequence 467 amino acids
Database Links
Entrez Gene 3664
SwissProt ID O14896
Protein Accession NP_006138
Application

Western blot

0.2-1 ug/mlELISA Titer: 1:312500Positive Control: Transfected 293T
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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