Sheep anti Human chx 10 (Visual system homeobox 2) (NT)
Product Specifications
Background
Chx10 is a 46kDa homeodomain protein of the paired-like class that is essential for development of the mammalian eye. Mutations in Chx10 cause microphthalmia, a cause of congenital blindness in Humans, and the ocular retardation (or) phenotype in mice. In the developing mouse retina Chx10 is expressed in retinal progenitors, while in the mature retina, Chx10 expression becomes restricted to bipolar neurons. Concurrent with these expression patterns, the Chx10-/- (or) retina is thin due to a defect in proliferation of retinal progenitors, and lacks bipolar neurons. Chx10 is also expressed in the developing brainstem, thalamus, and spinal cord.
Synonyms
Ceh-10 homeoDomain-containing homolog
UniProt
P58304
Host
Sheep
Species Reactivity
Human,Mouse,Rat,Chicken
Isotype
IgG
Conjugation
Unconjugated
Type
Polyclonal Antibody
Source
Antibody raised in sheep against a recombinant protein corresponding to amino acids 1 to 131 derived from the N-terminal region of the Human Chx10 protein conjugated to KLH.
Applications
WB, IHC (frozen)
Field of Research
Signal Transduction
Assay Principle
Detects Chx10 by Western blot at 0.5 to 1 µg/mL. Detects a 46 kDa band in mouse and rat retinal tissue lysates. Optimal concentration should be evaluated by serial dilutions. Suitable for use against recombinant proteins conjµgated to OVA, GST, His tags and other.
Stability
See expiration date on vial
Concentration
See vial for Concentration
Form
Ammonium sµLphate precipitated antibody in PBS with 0,08% sodium azide
Precautions
This product is intended FOR RESEARCH USE ONLY, and FOR TESTS IN VITRO, not for use in diagnostic or therapeutic procedures involving Humans or animals.
References & Citations
1. Liu, I.S., et al. Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer. Neuron 1994, 13, 377-393
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2. Chen, C.M. , Cepko, C.L. Expression of Chx10 and Chx10-1 in the developing chicken retina. Mech. Dev. 2000, 90, 293-297
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3. Ferda Percin, E., et al. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Nat. Genet. 2000, 25, 397-401_x000D_
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4. Nittner, D., et al. Synthetic lethality between Rb, p53 and Dicer or miR-17–92 in retinal progenitors suppresses retinoblastoma formation. Nature Cell Biology (2012), 14, 958-965 _x000D_
5. Kay, J.N., et al. Neurod6 expression defines new retinal amacrine cell subtypes and regulates their fate. Nature Neuroscience (2011), 14, 965-972_x000D_
6. Eiraku, M., et al. Self-organizing optic-cup morphogenesis in three-dimensional culture. Nature (2011), 472, 51-56
7. Pierfelice, T.J., et al. Notch3 Activation Promotes Invasive Glioma Formation in a Tissue Site-Specific Manner. Cancer Res., 71, 1115-1125 (2011)._x000D_
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7. Takae Kiyama, Ching-Kang Chen, Steven W Wang, Ping Pan, Zhenlin Ju, Jing Wang, Shinako Takada, William H Klein, Chai-An Mao_x000D_
Essential roles of mitochondrial biogenesis regulator Nrf1 in retinal development and homeostasis_x000D_
https://doi.org/10.1186/s13024-018-0287-z_x000D_
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8. Anastasia Marie Litke; Sarah Samuelson; Kerry R. Delaney; Yves Sauvé; Robert L. Chow_x000D_
Investigating the Pathogenicity of VSX1 Missense Mutations and Their Association With Corneal Disease_x000D_
Investigative Ophthalmology , Visual Science December 2018, Vol.59, 5824-5835. doi:10.1167/iovs.18-2549
Shipping Conditions
Ambient Temperature, freeze upon arrival
Storage Conditions
Product should be stored at -20ºC; Aliquot to avoid freeze/thaw cycles
Functional Analysis
WB
CAS Number
9007-83-4
Curated Selection
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