Product Name
LHX3, Blocking Peptide
Full Product Name
LHX3 Peptide - middle region
Product Gene Name
LHX3 blocking peptide
[Similar Products]
Product Synonym Gene Name
DKFZp762A2013; M2-LHX3; LIM3; CPHD3[Similar Products]
LHX3 peptide (MBS3226657) is used for blocking the activity of LHX3 antibody (MBS3201650)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q9UBR4
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of LHX3 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
LHX3 blocking peptide
This is a synthetic peptide designed for use in combination with anti-LHX3 antibody made
Target Description: LHX3 encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. This gene encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. Two transcripts variants encoding distinct isoforms have been identified for this gene.
Product Categories/Family for LHX3 blocking peptide
Peptide
Applications Tested/Suitable for LHX3 blocking peptide
Western Blot (WB)
NCBI/Uniprot data below describe general gene information for LHX3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_055379
[Other Products]
NCBI GenBank Nucleotide #
NM_014564
[Other Products]
UniProt Primary Accession #
Q9UBR4
[Other Products]
UniProt Related Accession #
Q9UBR4[Other Products]
NCBI Official Full Name
LIM/homeobox protein Lhx3 isoform b
NCBI Official Synonym Full Names
LIM homeobox 3
NCBI Official Symbol
LHX3 [Similar Products]
NCBI Official Synonym Symbols
LIM3; CPHD3; M2-LHX3
[Similar Products]
NCBI Protein Information
LIM/homeobox protein Lhx3
UniProt Protein Name
LIM/homeobox protein Lhx3
Protein Family
LIM/homeobox protein
UniProt Gene Name
LHX3 [Similar Products]
UniProt Synonym Gene Names
LIM homeobox protein 3 [Similar Products]
UniProt Entry Name
LHX3_HUMAN
NCBI Summary for LHX3
This gene encodes a member of a large family of proteins which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene cause combined pituitary hormone deficiency 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
UniProt Comments for LHX3
LHX3: Acts as a transcriptional activator. Binds to and activates the promoter of the alpha-glycoprotein gene, and synergistically enhances transcription from the prolactin promoter in cooperation with Pit-1. Defects in LHX3 are the cause of pituitary hormone deficiency combined type 3 (CPHD3); also known as combined pituitary hormone deficiency with rigid cervical spine or sensorineural deafness with pituitary dwarfism. CPHD is characterized by a complete deficit in all but one (adrenocorticotropin) anterior pituitary hormone and a rigid cervical spine leading to limited head rotation. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: DNA-binding; Transcription factor
Chromosomal Location of Human Ortholog: 9q34.3
Cellular Component: transcription factor complex; nucleus
Molecular Function: zinc ion binding; sequence-specific DNA binding
Biological Process: transcription from RNA polymerase II promoter; organ morphogenesis; pituitary gland development; positive regulation of transcription, DNA-dependent; spinal cord motor neuron cell fate specification; spinal cord association neuron differentiation; motor axon guidance; positive regulation of transcription from RNA polymerase II promoter; medial motor column neuron differentiation; ventral spinal cord interneuron specification; inner ear development; negative regulation of apoptosis; placenta development; lung development
Disease: Pituitary Hormone Deficiency, Combined, 3
Research Articles on LHX3
1. Study did not identify HESX1 and LHX3 mutations by Sanger in brazilian patients with combined pituitary hormone deficiency
Precautions
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Disclaimer
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