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CRX Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of CRX antibodies. Select CRX antibodies from several monoclonal and/or polyclonal CRX antibodies listed below. View detailed CRX antibody specifications by linking to the specific product blocks. Select appropriate CRX antibodies for your research by isotype, epitope, applications and species reactivity. CRX gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available.

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PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
CRX (A-9)sc-377138mouse IgG1111-143 (h)WB, IP, IF, ELISAm, r, h
CRX (A-14)sc-22380goat IgGinternal (h)WB, IP, IF, ELISAm, r, h
CRX (B-11)sc-377207mouse IgG1166-285 (h)WB, IP, IF, ELISAm, h
CRX (G-18)sc-22381goat IgGC-terminus (h)WB, IF, IPELISAm, r, h, c, b, p
CRX (H-120)sc-30150rabbit IgG166-285 (h)WB, IP, IF, ELISAm, r, h, c, b, p4
CRX (Q17)sc-81958mouse IgG2aFL (h)WB, IP, ELISAhuman1

CRX siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
CRX siRNA (h): sc-38649CRX shRNA Plasmid (h):
sc-38649-SH
CRX shRNA (h)
Lentiviral Particles: sc-38649-V
CRX siRNA (m): sc-38650CRX shRNA Plasmid (m):
sc-38650-SH
CRX shRNA (m)
Lentiviral Particles: sc-38650-V

The cone-rod homeobox-containing gene (CRX) encodes a transcription factor that coordinates the expression of several photoreceptor genes in the developing retina, including opsin and rhodopsin. Specifically, CRX binds the OTX motif (TAATCC/A) upstream from photoreceptor genes. The CRX gene is also expressed in the pinealocytes of the pineal gland and may regulate pineal circadian activity by controling the expression of melatonin synthesis genes. Furthermore, CRX(-) mice exhibit disruption of circadian rhythms. The human CRX gene maps to chromosome 19q13.3 within the region of the cone-rod dystrophy-2 locus (CORD2). Mutations in the CRX gene are implicated in the visual pathologies of CORD, Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP). All characterized CRX gene mutations produce disease in heterozygotes although there is no known correlation between the pathologic phenotype and genetic mutation. Missense mutations of the CRX gene affect the homeobox domain, whereas frameshift mutations affect the OTX domain.