LCA5 Rabbit Polyclonal Antibody
No Size Price Availability  
YRP09978-01 50ul 1500.00 In Stock
YRP09978-01 100ul 2000.00 In Stock
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Source: Rabbit Gene Id: 167691
Isotype: IgG Swiss Prot:
purity: Purified by Protein A.
Background:
Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.
Reactivity Human, Mouse, Rat
Tested applications WB IHC IF
Clonality Polyclonal Antibody
Calculated MW /
Recommended Dilutions
WB 1:100-1:1000
IHC 1:100-1:500
IF 1:50-1:200
Immunogen KLH conjugated synthetic peptide derived from human LCA5
Storage Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at -20℃ for 12 months
Synonym C6orf152, LCA5, Leber congenital amaurosis 5, Leber congenital amaurosis 5 protein, ORF64, RGD1308555.
This product is for research use only, not for diagnostic or therapeutic use!

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