LCA5 Polyclonal antibody

LCA5 Polyclonal Antibody for WB, ELISA
Cat No. 19333-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human and More (2)

应用

WB, ELISA and More (2)

C6orf152, LCA5, Leber congenital amaurosis 5, Lebercilin

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inHeLa cells

推荐稀释比

应用推荐稀释比
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

19333-1-AP targets LCA5 in WB, IF, CoIP, ELISA applications and shows reactivity with human samples.

经测试应用 WB, ELISA Application Description
文献引用应用WB, IF, CoIP
经测试反应性 human
文献引用反应性human, mouse, pig
免疫原 LCA5 fusion protein Ag5140 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 Leber congenital amaurosis 5
别名 C6orf152, LCA5, Leber congenital amaurosis 5, Lebercilin
计算分子量 693 aa, 80 kDa
观测分子量 80 kDa
GenBank蛋白编号BC050327
基因名称 LCA5
Gene ID (NCBI) 167691
RRIDAB_2878576
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ86VQ0
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件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
WB protocol for LCA5 antibody 19333-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
mouse

Mol Ther

Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness.

Authors - Ji Yun Song
mouseIF

Hum Mol Genet

Disruption of the Retinitis Pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration.

Authors - Marcus Karlstetter
mouseIF

Invest Ophthalmol Vis Sci

Treatment Potential for LCA5-Associated Leber Congenital Amaurosis.

Authors - Katherine E Uyhazi
pigIF

J Proteomics

Tissue- and isoform-specific protein complex analysis with natively processed bait proteins.

Authors - Tina Beyer
humanWB,IF,CoIP

Sci Rep

The interaction between LC8 and LCA5 reveals a novel oligomerization function of LC8 in the ciliary-centrosome system

Authors - Tamás Szaniszló
humanIF

Nat Commun

iU-ExM: nanoscopy of organelles and tissues with iterative ultrastructure expansion microscopy

Authors - Vincent Louvel
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