LCA5L Polyklonale Antilichaam, AbBy FluorTM 555 Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.
C21ORF13; Chromosome 21 open reading frame 13; Lca5l; LCA5L_HUMAN; Leber congenital amaurosis 5 like; Leber congenital amaurosis 5 like protein; Leber congenital amaurosis 5-like protein; Lebercilin-like protein.
150082
O95447
• Rabbit
301-400/670
LCA5L
• Polyclonal
• IgG
AbBy Fluor™ 555
KLH conjugated synthetic peptide derived from human LCA5L
WB, IF (IHC-P)
Purified by Protein A.
553nm/568nm
1µg/µl
WB (1:300-5000), IF (IHC-P) (1:50-200)
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Unmodified
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
150082
Human, Mouse, Rat, Cow, Sheep, Pig, Horse, Rabbit
Beschrijving
LCA5L Polyklonale Antilichaam, AbBy FluorTM 555 Vervoeging Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
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