Human DLX1 Matched Antibody Pair Set [ABP-Q-0554] (CAT#: ABP-Q-0554)

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Human DLX1 Matched Antibody Pair set for ELISA useCapture Antibody: Mouse monoclonal anti-DLX1Detection Antibody: Rabbit purified polyclonal anti-DLX1

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Antigen Detail

TargetDLX1
DescriptionDistal-less homeobox 1(DLX1) is a member of the DLX family of homeobox transcription factors, which is essential for the production of forebrain GABAergic interneurions during embryonic development. The DLX family of homeobox transcription factors (Dlx1, Dlx2, Dlx5 and Dlx6) is expressed in overlapping domains at different stages of cell differentiation in the subpallium and controls differentiation of GABAergic neurons. DLX1 possible has a role in craniofacial patterning and morphogenesis and involves in the early development of diencephalic subdivisions.
Species ReactivityHuman

Capture Antibody

Capture ClonalityMonoclonal
Host SpeciesMouse
CloneIV01260
PurificationAffinity chromatography
BufferPBS, pH 7.4, containing 0.1% Proclin 300
ApplicationELISA

Detection Antibody

Det-ClonalityPolyclonal
Host SpeciesRabbit
ConjugationUnconjugated
PurificationAffinity chromatography
BufferPBS, pH 7.4

General Product Property

Product OverviewHuman DLX1 Matched Antibody Pair set for ELISA use
Capture Antibody: Mouse monoclonal anti-DLX1
Detection Antibody: Rabbit purified polyclonal anti-DLX1
SpecificityValidated for detecting natural and recombinant human DLX1
Research AreaNeurology process
ApplicationELISA
Application NotesOptimal dilutions should be determined experimentally by the user.
FormLyophilized
StorageAvoid repeated freeze/thaw cycles. Store at 2-8°C for short term. Aliquot and store at -20°C for long term storage.
Size1 Set
Sample TypeSerum; Supernatant; Urine; Cell lysate; Plasma; Tissue Homogenates
Usage StatementAvailable for Research Use Only. Not for use in therapeutic or diagnostic applications.

Target Overview

Gene SymbolDLX1
Full NameDistal-Less Homeobox 1
BackgroundThis gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein is localized to the nucleus where it may function as a transcriptional regulator of signals from multiple TGF-{beta} superfamily members. The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain. This gene is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 2. Alternatively spliced transcript variants encoding different isoforms have been described.
Alternative NamesHomeobox Protein DLX-1
Gene ID1745
Uniprot IDP56177
GeneCardsDLX1
HGNC2914
EnsemblENSG00000144355
OMIM600029
Involvement in DiseaseDiseases associated with DLX1 include Dental Fluorosis and Witkop Syndrome.
FunctionPlays a role as a transcriptional activator or repressor (PubMed:14671321). Inhibits several cytokine signaling pathways, such as TGFB1, activin-A/INHBA and BMP4 by interfering with the transcriptional stimulatory activity of transcription factors, such as MSX2, FAST2, SMAD2 and SMAD3 during hematopoietic cell differentiation (PubMed:14671321). Plays a role in terminal differentiation of interneurons, such as amacrine and bipolar cells in the developing retina (By similarity). Likely to play a regulatory role in the development of the ventral forebrain (By similarity). May play a role in craniofacial patterning and morphogenesis and may be involved in the early development of diencephalic subdivisions (By similarity).
Related PathwaysIts related pathways are DNA Damage/Telomere Stress Induced Senescence and Regulation of nuclear SMAD2/3 signaling.

For Research Use Only.

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