LCA5 Antibody (PACO37306)
- SKU:
- PACO37306
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- Applications:
- WB
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Description
| Antibody Name: | LCA5 Antibody (PACO37306) |
| Antibody SKU: | PACO37306 |
| Size: | 50ug |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, WB |
| Recommended Dilutions: | ELISA:1:2000-1:10000, WB:1:1000-1:5000 |
| Species Reactivity: | Human, Mouse |
| Immunogen: | Recombinant Human Lebercilin protein (101-400AA) |
| Form: | Liquid |
| Storage Buffer: | Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 |
| Purification Method: | >95%, Protein G purified |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | Western blot. All lanes: LCA5 antibody at 18µg/ml + Mouse kidney tissue. Secondary. Goat polyclonal to rabbit IgG at 1/10000 dilution. Predicted band size: 81 kDa. Observed band size: 81 kDa. |
| Background: | Might be involved in minus end-directed microtubule transport. |
| Synonyms: | Lebercilin (Leber congenital amaurosis 5 protein), LCA5, C6orf152 |
| UniProt Protein Function: | 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 functionChromosomal Location of Human Ortholog: 6q14.1Cellular Component: axoneme; ciliumMolecular Function: protein binding; protein complex bindingBiological Process: intraflagellar transport; photoreceptor cell maintenanceDisease: Leber Congenital Amaurosis 5 |
| UniProt Protein Details: | |
| NCBI Summary: | 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 Code: | Q86VQ0 |
| NCBI GenInfo Identifier: | 170650672 |
| NCBI Gene ID: | 167691 |
| NCBI Accession: | NP_001116241.1 |
| UniProt Secondary Accession: | Q86VQ0,Q9BWX7, E1P542 |
| UniProt Related Accession: | Q86VQ0 |
| Molecular Weight: | 80,554 Da |
| NCBI Full Name: | lebercilin |
| NCBI Synonym Full Names: | Leber congenital amaurosis 5 |
| NCBI Official Symbol: | LCA5 |
| NCBI Official Synonym Symbols: | C6orf152 |
| NCBI Protein Information: | lebercilin |
| UniProt Protein Name: | Lebercilin |
| UniProt Synonym Protein Names: | Leber congenital amaurosis 5 protein |
| Protein Family: | Lebercilin |
| UniProt Gene Name: | LCA5 |
| UniProt Entry Name: | LCA5_HUMAN |
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