LCA5 Proteins

(Leber Congenital Amaurosis 5 (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].

Recommended next Filters:

All filter options

Would you like to try our new AI Search?

Show Filters

5 results

LCA5 Protein (AA 1-704) (His tag)

custom-made LCA5 Origin: Mouse Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)

AlphaFold protein structure predicition of Mouse Recombinant Lca5 Protein, UniprotID Q80ST9

3 images

Catalog No. ABIN7558309

Details

LCA5 Protein (AA 1-697) (His tag)

custom-made LCA5 Origin: Human Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)

AlphaFold protein structure predicition of Human Recombinant LCA5 Protein, UniprotID Q86VQ0

3 images

Catalog No. ABIN7549004

Details

LCA5 Protein (AA 1-704) (Strep Tag)

custom-made LCA5 Origin: Mouse Host: Cell-free protein synthesis (CFPS) Recombinant approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC). ELISA, SDS, WB

Catalog No. ABIN3124226

Details

LCA5 Protein (AA 1-697) (Strep Tag)

custom-made LCA5 Origin: Human Host: Cell-free protein synthesis (CFPS) Recombinant approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC). ELISA, SDS, WB

Catalog No. ABIN3082870