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

Cat No : 19333-1-AP

Print datasheet

Synonyms

C6orf152, LCA5, Leber congenital amaurosis 5, Lebercilin



经过测试的应用

Positive WB detected inHeLa cells

推荐稀释比

ApplicationDilution
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
Cited ApplicationsWB, IF, CoIP
Tested Reactivity human
Cited Reactivityhuman, 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 NumberBC050327
Gene Symbol LCA5
Gene ID (NCBI) 167691
RRIDAB_2878576
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDQ86VQ0
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore 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