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The protein encoded by CRX is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. Additionally we are shipping Cone-Rod Homeobox Proteins (8) and many more products for this protein.
Showing 10 out of 42 products:
Human Monoclonal CRX Primary Antibody for ELISA, WB - ABIN560473
Peng, Chen: Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation. in Human molecular genetics 2007
Show all 9 references for ABIN560473
Human Monoclonal CRX Primary Antibody for RNAi, ELISA - ABIN560472
Gong, Sagiv, Cai, Tsang, Del Priore: Effects of extracellular matrix and neighboring cells on induction of human embryonic stem cells into retinal or retinal pigment epithelial progenitors. in Experimental eye research 2008
CRX can influence the development and opsin (show RHO Antibodies) expression of photoreceptor outer segments in zebrafish.
The CRX protein can recognize the BAT 1 (show DDX39B Antibodies) regulatory region contains highly conserved OTX (GATTA) and OTX-like (TATTA) sequences.
No mutation in crx were identified in homozygous mok(m632) or nie(m743). Consistent with the absence of identified mutations, linkage analysis excluded linkage of the mutant phenotypes to crx.
data demonstrate the successful application of ZFN technology to generate CRX-GFP labeled hESC lines, which can be used to study and isolate photoreceptor precursors during hESC differentiation.
Loss of OTX2 (show OTX2 Antibodies) expression resulted in decreased expression of C-MYC (show MYC Antibodies) and CRX, genes previously implicated in retinoblastoma tumorigenesis. Loss of OTX2 (show OTX2 Antibodies) expression increased the phosphorylation of RB, a potential mechanism of modulating cell proliferation
Mutations involving the CRX gene may demonstrate an autosomal dominant inheritance pattern for leber congenital amaurosis.
Con (show DISP1 Antibodies) rod homeobox protein mRNA is a novel marker for retinoblastoma at extraocular sites.
Two de novo mutations in CRX were found in Chinese patients with Leber congenital amaurosis. The CRX mutation might create a dominantly inherited trait.
Mutations in CRX demonstrate significant phenotypic heterogeneity both between and within pedigrees. A novel, adult-onset, macular dystrophy phenotype is characterized, further extending our knowledge of the etiology of dominant macular dystrophies.
CRX could be useful in surgical neuropathology for the differential diagnosis of pineal region tumors, in particular to discriminate pineal tumors from glial tumors
Data have identified a novel retinal SAM (show TTN Antibodies) domain protein, Samd7, which could act as a transcriptional repressor involved in fine-tuning of Crx-regulated gene expression.
the potential utility of CRX as a marker of pineal lineage in routine diagnostic neuropathology.
These findings suggest that CRX is a useful marker to discriminate metastatic retinoblastoma from other, more common, malignant small round cell tumors of childhood
OTR1 (show OXTR Antibodies), OTX2 (show OTX2 Antibodies) and CRX act as positive modulators of the BEST1 (show BEST1 Antibodies) promoter in the retinal pigment epithelium.
CRX-associated retinopathies stem from graded changes in photoreceptor gene expression, which could significantly contribute to phenotypic variability.
Rax (show RAX Antibodies) and Crx cooperatively transactivate Rhodopsin (show RHO Antibodies) and cone opsin (show RHO Antibodies) promoters and an optimum Rax (show RAX Antibodies) expression level to transactivate photoreceptor gene expression exists.
E168d2 and R90W are mechanistically distinct mouse models for CRX-associated disease that will allow the elucidation of molecular mechanisms and testing of novel therapeutic approaches for different forms of CRX-associated disease.
The rhythmic nature of pineal CRX protein may directly modulate the daily profile of Aanat (show AANAT Antibodies) expression by inducing nighttime expression of this enzyme, facilitating nocturnal melatonin synthesis
We conclude that nucleotide changes in evolutionary conserved crx binding site could impact retina-specific expression levels of Kcnv2 (show KCNV2 Antibodies).
In Crx-knockout mice vasopressin (show AVP Antibodies) mRNA expression in the suprachiasmatic nucleus shows significant daily rhythm.
Our results show that NRL (show NRL Antibodies) and CRX together control the expression of most, if not all, genes involved in rod phototransduction through a cis (show CISH Antibodies)-regulatory module
Crx broadly modulates the pineal transcriptome and also influences differential night/day gene expression in this tissue
A change in the suprachiasmatic nuclei of the Crx-deficient mouse might explain the observed circadian differences between the knockout mouse and wild-type mouse.
The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.
, homeobox protein otx5
, orthodenticle homolog 5
, cone-rod homeobox protein
, orthodenticle homeobox 3
, crx gene for cone-rod homeobox protein
, photoreceptor-specific cone-rod homeobox protein
, cone-rod homeobox containing