LCA5 Polyclonal antibody
LCA5 Polyclonal Antibody for WB, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human and More (2)
Applications
WB, ELISA and More (2)
Conjugate
Unconjugated
验证数据展示
经过测试的应用
Positive WB detected in | HeLa cells |
推荐稀释比
Application | Dilution |
---|---|
Western Blot (WB) | WB : 1:200-1:1000 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
The immunogen of 19333-1-AP is LCA5 Fusion Protein expressed in E. coli.
Tested Applications | WB, ELISA Application Description |
Cited Applications | WB, IF, CoIP |
Tested Reactivity | human |
Cited Reactivity | human, mouse, pig |
Immunogen | LCA5 fusion protein Ag5140 种属同源性预测 |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Full Name | Leber congenital amaurosis 5 |
Synonyms | C6orf152, LCA5, Leber congenital amaurosis 5, Lebercilin |
Calculated Molecular Weight | 693 aa, 80 kDa |
Observed Molecular Weight | 80 kDa |
GenBank Accession Number | BC050327 |
Gene Symbol | LCA5 |
Gene ID (NCBI) | 167691 |
RRID | AB_2878576 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
UNIPROT ID | Q86VQ0 |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
LCA5 (Leber congenital amaurosis 5), also named as C6orf152 or Lebercilin, is a 697 amino acids protein. LCA5 is widely expressed at the microtubules, centrosome, and primary cilia. Recent study showed that LCA5 was involved in the cause of congenital and early-onset retinal dystrophies (PMID: 24144451). The MW of this protein is 80 kDa, and this antibody specially recognises the 80 kDa protein.
实验方案
Product Specific Protocols | |
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WB protocol for LCA5 antibody 19333-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
发表文章
Species | Application | Title |
---|---|---|
Mol Ther Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness. | ||
Hum Mol Genet Disruption of the Retinitis Pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration. | ||
Invest Ophthalmol Vis Sci Treatment Potential for LCA5-Associated Leber Congenital Amaurosis. | ||
J Proteomics Tissue- and isoform-specific protein complex analysis with natively processed bait proteins. | ||
Sci Rep The interaction between LC8 and LCA5 reveals a novel oligomerization function of LC8 in the ciliary-centrosome system | ||
Nat Commun iU-ExM: nanoscopy of organelles and tissues with iterative ultrastructure expansion microscopy |