AIPL1 Rabbit anti-Human, Mouse, Rat, Polyclonal Antibody, Abnova™

Rabbit polyclonal antibody raised against synthetic peptide of AIPL1.

Supplier:  Abnova Corporation PAB16585

Catalog No. 89-118-456

Description

Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is the most severe inherited retinopathy with the earliest age of onset. Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram. The photoreceptor/pineal -expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, was mapped within the LCA4 candidate region. The protein contains three tetratricopeptide motifs, consistent with nuclear transport or chaperone activity. AIPL1 mutations may cause approximately 20% of recessive LCA. [provided by RefSeq

Specifications

• Antigen: AIPL1
• Classification: Polyclonal
• Description: Rabbit polyclonal antibody raised against synthetic peptide of AIPL1.
• Formulation: In PBS (0.02% sodium azide)
• Gene Accession No.: NP_055151
• Gene Symbols: AIPL1
• Immunogen: A synthetic peptide corresponding to internal region 18 amino acids of human AIPL1.
• Regulatory Status: RUO
• Gene ID (Entrez): 23746
• Content And Storage: Store at 4°C for three months. For long term storage store at -20°C.
  Aliquot to avoid repeated freezing and thawing.

• Applications: ELISA, Immunohistochemistry, Western Blot
• Conjugate: Unconjugated
• Dilution: Western Blot (1-2 ug/mL) The optimal working dilution should be determined by the end user.
• Gene: AIPL1
• Gene Alias: AIPL2/LCA4
• Host Species: Rabbit
• Quantity: 100 μg
• Primary or Secondary: Primary
• Target Species: Human, Mouse, Rat
• Form: Liquid

For Research Use Only