Leber Congenital Amaurosis 5 (LCA5) Peptide
LCA5
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all LCA5 products
- LCA5 (Leber Congenital Amaurosis 5 (LCA5))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-LCA5 antibody (Catalog #: ARP53410_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- LCA5 (Leber Congenital Amaurosis 5 (LCA5))
- Synonyms
- C6orf152 Peptide, RGD1308555 Peptide, 4930431B11Rik Peptide, 5730406O13Rik Peptide, AV274874 Peptide, ORF64 Peptide, LCA5, lebercilin Peptide, Leber congenital amaurosis 5 Peptide, Leber congenital amaurosis 5 (human) Peptide, LCA5 Peptide, LOC787523 Peptide, Lca5 Peptide
- Background
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LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. 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. Alternative splicing results in two transcript variants.
Alias Symbols: C6orf152
Protein Size: 697 - Molecular Weight
- 80 kDa
- Gene ID
- 167691
- NCBI Accession
- NM_181714, NP_859065
- UniProt
- Q86VQ0
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