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LCA5 Polyclonal antibody

LCA5 Polyclonal Antibody for WB, ELISA

Cat No. 19333-1-AP

Host / Isotype

Rabbit / IgG

Reactivity

human and More (2)

Applications

WB, IF, CoIP, ELISA

C6orf152, Leber congenital amaurosis 5, Lebercilin

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 
SKU: 

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Freight/Packing: -

Quantity

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Tested Applications

Positive WB detected inHeLa cells

Recommended dilution

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.

Product Information

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

Tested Reactivity human
Cited Reactivityhuman, mouse, pig
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag5140

Product name: Recombinant human LCA5 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 4-283 aa of BC050327

Sequence: RAGSPGTDQEREAGKHHYSYSSDFETPQSSGRSSLVSSSPASVRRKNPKRQTSDGQVHHQAPRKPSPKGLPNRKGVRVGFRSQSLNREPLRKDTDLVTKRILSARLLKINELQNEVSELQVKLAELLKENKSLKRLQYRQEKALNKFEDAENEISQLIFRHNNEITALKERLRKSQEKERATEKRVKDTESELFRTKFSLQKLKEISEARHLPERDDLAKKLVSAELKLDDTERRIKELSKNLELSTNSFQRQLLAERKRAYEAHDENKVLQKEVQRLYH

Predict reactive species
Full Name Leber congenital amaurosis 5
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
FormLiquid
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. 20ul sizes contain 0.1% BSA.

Background Information

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.

Protocols

Product Specific Protocols
WB protocol for LCA5 antibody 19333-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

What published studies show

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
mouseIF

EMBO Mol Med

Fine-tuning FAM161A gene augmentation therapy to restore retinal function

Authors - Yvan Arsenijevic
mouseIF

EMBO J

Glutamylation imbalance impairs the molecular architecture of the photoreceptor cilium

Authors - Olivier Mercey
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