Product Name
LCA5, Polyclonal Antibody
Popular Item
Full Product Name
LCA5 Antibody
Product Synonym Names
Lebercilin; Leber congenital amaurosis 5 protein; LCA5; C6orf152
Product Gene Name
anti-LCA5 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q86VQ0
Purity/Purification
>95%,Protein G purified
Immunogen
Recombinant human Lebercilin protein
Conjugation
Non-conjugated
Storage Buffer
Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-133728
Preparation and Storage
Shipped at 4 degree C. Upon delivery, aliquot and store at -20 degree C or -80 degree C.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-LCA5 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-LCA5 antibody
Might be involved in minus end-directed microtubule transport.
Applications Tested/Suitable for anti-LCA5 antibody
ELISA (EIA), Western Blot (WB)
Western Blot (WB) of anti-LCA5 antibody
Western blot
All lanes: LCA5 antibody at 18 ug/ml+Mouse kidney tissue
Goat polyclonal to rabbit at 1/10000 dilution
Predicted band size: 81 kDa
Observed band size: 81 kDa

NCBI/Uniprot data below describe general gene information for LCA5. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001116241.1
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NCBI GenBank Nucleotide #
NM_001122769.2
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UniProt Primary Accession #
Q86VQ0
[Other Products]
UniProt Secondary Accession #
Q9BWX7; E1P542[Other Products]
UniProt Related Accession #
Q86VQ0[Other Products]
Molecular Weight
80,554 Da
NCBI Official Full Name
lebercilin
NCBI Official Synonym Full Names
Leber congenital amaurosis 5
NCBI Official Symbol
LCA5 [Similar Products]
NCBI Official Synonym Symbols
C6orf152
[Similar Products]
NCBI Protein Information
lebercilin
UniProt Protein Name
Lebercilin
UniProt Synonym Protein Names
Leber congenital amaurosis 5 protein
Protein Family
Lebercilin
UniProt Gene Name
LCA5 [Similar Products]
UniProt Synonym Gene Names
C6orf152 [Similar Products]
UniProt Entry Name
LCA5_HUMAN
NCBI Summary for LCA5
This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]
UniProt Comments for LCA5
LCA5: Might be involved in minus end-directed microtubule transport. Defects in LCA5 are the cause of Leber congenital amaurosis type 5 (LCA5). LCA designates a clinically and genetically heterogeneous group of childhood retinal degenerations, generally inherited in an autosomal recessive manner. Affected infants have little or no retinal photoreceptor function as tested by electroretinography. LCA represents the most common genetic cause of congenital visual impairment in infants and children. Belongs to the LCA5 family.
Protein type: Unknown function
Chromosomal Location of Human Ortholog: 6q14.1
Cellular Component: axoneme; cilium
Molecular Function: protein binding; protein complex binding
Biological Process: intraflagellar transport; photoreceptor cell maintenance
Disease: Leber Congenital Amaurosis 5
Research Articles on LCA5
1. Identification of novel LCA5 mutations in patients with Leber congenital amaurosis and retinitis pigmentosa.
Precautions
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