21号染色体开放阅读框13抗体

Quantity size:

0.2ml

Concentration:

1mg/ml 21号染色体开放阅读框13抗体  Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

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 21号染色体开放阅读框13抗体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 21号染色体开放阅读框13抗体of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.

Also known as:

C21orf13; Chromosome 21 open reading frame 13; Lca5l; LCA5L_HUMAN; Leber congenital amaurosis 5 like; Leber congenital amaurosis 5 like protein; Leber congenital amaurosis 5-like protein; Lebercilin-like protein;21号染色体开放阅读框13抗体 MGC33295; OTTHUMP00000069084; OTTHUMP00000069085.

Specificity:

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Rabbit Polyclonal IgG, affinity purified by Protein A.

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Reacts with: Human, Mouse, Rat, Horse, .

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Immunogen: KLH conjugated synthetic peptide derived from human C21ORF13.

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21号染色体开放阅读框13抗体Predicted Molecular Weight: 77kDa.

Storage:

Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).

Application:

WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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