DLX1 Antibody

Code CSB-PA006952GA01HU
Size $600
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Product Details

Uniprot No.
Target Names
DLX1
Alternative Names
DII B antibody; Distal less homeo box 1 antibody; Distal less homeobox 1 antibody; Distal-less homeobox gene 1a antibody; Dlx 1 antibody; Dlx antibody; Dlx1 antibody; Dlx1 distal-less homeobox 1 antibody; DLX1_HUMAN antibody; Homeo box protein DLX1 antibody; Homeobox protein DLX 1 antibody; Homeobox protein DLX-1 antibody; Homeobox protein Dlx1a antibody; Homeodomain transcription factor DLX1 antibody; MGC189409 antibody; OTTHUMP00000082494 antibody; OTTHUMP00000082497 antibody; OTTMUSP00000014202 antibody; RP23-419H3.3 antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Human DLX1
Immunogen Species
Homo sapiens (Human)
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Plays a role as a transcriptional activator or repressor. 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. Plays a role in terminal differentiation of interneurons, such as amacrine and bipolar cells in the developing retina. Likely to play a regulatory role in the development of the ventral forebrain. May play a role in craniofacial patterning and morphogenesis and may be involved in the early development of diencephalic subdivisions.
Gene References into Functions
  1. observations suggest that altered DLX1 methylation and expression contribute to pathogenesis of PSP by influencing MAPT. PMID: 30050033
  2. Our results provided evidence that polymorphisms in TIMP1, DLX1 and DLX2 genes may be associated with DF phenotypes. PMID: 28131910
  3. DLX1 mRNA levels were shown to be good predictors for the detection of High-grade Prostate Cancer. PMID: 27108162
  4. these data strongly suggest that DLX1 has a pivotal role in FOXM1 signaling to promote cancer aggressiveness through intensifying TGF-beta/SMAD4 signaling in high-grade serous ovarian cancer cells. PMID: 27593933
  5. TDT results showed an association between DLX1 and cleft lip and palate, in which the A allele was undertransmited (p=0.022). PMID: 25463899
  6. The study data demonstrate an association between SNP rs7888172 of the DLX1 gene and non-syndromic hypodontia in Chinese Han individuals. PMID: 22984994
  7. The regulation of fate switch between cortical and striatal interneurons is dependent on Dlx1 (and Dlx2). PMID: 23312518
  8. These findings suggest that alterations in DLX1/2 contribute to the biological consequences of FLT3 activation. PMID: 21357706
  9. DLX1 may function as a regulator of multiple signals from TGF-beta superfamily members in broad biological contexts during blood production PMID: 14671321
  10. The DLX1 and DLX2 genes lie head-to-head in 2q32; the findings support the presence of two functional polymorphisms, one in or near each of the DLX genes that increase susceptibility to, or cause, autism. PMID: 18728693

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Subcellular Location
Nucleus.
Protein Families
Distal-less homeobox family
Tissue Specificity
Expressed in hematopoietic cell lines.
Database Links

HGNC: 2914

OMIM: 600029

KEGG: hsa:1745

STRING: 9606.ENSP00000354478

UniGene: Hs.407015

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