Welcome to Omnimabs!
TEL: 02154156726 Info: info@Omnimabs.com CN

Rabbit anti-PITX2 polyclonal antibody - N-terminal region

Catalog Number:OM105798
OM105798
Discount Price
OM105798-100ul
1~2 Week
100ul
OM105798-50ul
50ul
OM105798-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-PITX2 polyclonal antibody - N-terminal region
Antibody Type Primary Antibodies
Antigen Alias ARP1, Brx1, IDG2, IGDS, IGDS2, IHG2, IRID2, MGC111022, MGC20144, Otlx2, PTX2, RGS, RIEG, RIEG1, RS
Immunogen The immunogen for anti-PITX2 antibody: synthetic peptide directed towards the N terminal of human PITX2
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 DogHorseHumanMouseRat
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol PITX2
Gene Synonyms ARP1
Brx1
IDG2
IGDS
IGDS2
IHG2
IRID2
MGC111022
MGC20144
Otlx2
PTX2
RGS
RIEG
RIEG1
RS
Gene Full Name Paired-like homeodomain 2
Gene Summary The PITX2 gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. This protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. Mutations in PITX2 are associated with Axenfeld-Rieger syndrome (ARS), iridogoniodysgenesis syndrome (IGDS), and sporadic cases of Peters anomaly. This protein is involved in the development of the eye, tooth and abdominal organs. It also acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described.
Alternative Names ARP1
Brx1
IDG2
IGDS
IGDS2
IHG2
IRID2
MGC111022
MGC20144
Otlx2
PTX2
RGS
RIEG
RIEG1
RS
Molecular Weight(MW) 35kDa
Sequence 317 amino acids
Database Links
Entrez Gene 5308
SwissProt ID Q99697
Protein Accession NP_700475
Application

Western blot

0.2-1 ug/mlELISA Titer: 1:31250Positive Control: Human heart
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.
validation
question title
question detaiil
Verification code