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LCA5 Products

(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].

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Featured LCA5 Categories

LCA5 Antibodies

High quality antibodies with extensive validation data.

LCA5 ELISA Kits

Reliable ELISA kits for a wide range of species.

LCA5 Proteins

Proteins for various applications incl. WB, ELISA, IF etc.

Recommended LCA5 Antibodies

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Cow, Dog, Guinea Pig, Horse, Human, Mouse, Rabbit, Rat
Application WB
Validations
  • (1)
  • (1)
Cat. No. ABIN2785382
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application ELISA, WB
Validations
  • (1)
Cat. No. ABIN7157958
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (1)
Cat. No. ABIN632308
Quantity 100 μL
Datasheet Datasheet

Recommended LCA5 ELISA Kits

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method
Validations
Cat. No. ABIN1140109
Quantity 96 tests
Datasheet Datasheet
Reactivity Mouse
Analytical Method
Validations
Cat. No. ABIN1140110
Quantity 96 tests
Datasheet Datasheet
Reactivity Rat
Analytical Method
Validations
Cat. No. ABIN1140111
Quantity 96 tests
Datasheet Datasheet

Recommended LCA5 Proteins

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3082870
Quantity 1 mg
Datasheet Datasheet
Reactivity Mouse
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3124226
Quantity 1 mg
Datasheet Datasheet
Reactivity Human
Source Escherichia coli (E. coli)
Validations
Cat. No. ABIN7123727
Quantity 50 μg
Datasheet Datasheet

Latest Publications for our LCA5 products

Ramprasad, Soumittra, Nancarrow, Sen, McKibbin, Williams, Arokiasamy, Lakshmipathy, Inglehearn, Kumaramanickavel: "Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis." in: Molecular vision, Vol. 14, pp. 481-6, (2008) (PubMed).

Synonyms and alternative names related to LCA5

LCA5, lebercilin (LCA5), Leber congenital amaurosis 5 (LOC787523), LCA5, lebercilin (Lca5), Leber congenital amaurosis 5 (human) (Lca5), 4930431B11Rik, 5730406O13Rik, AV274874, C6orf152, ORF64, RGD1308555

Protein level used designations for LCA5

  • Leber congenital amaurosis 5
  • lebercilin-like
  • Lebercilin
  • leber congenital amaurosis 5 protein
  • leber congenital amaurosis 5 protein homolog
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