AIPL1 anticorps (C-Term)
Aperçu rapide pour AIPL1 anticorps (C-Term) (ABIN5515809)
Antigène
Voir toutes AIPL1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term
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Fonction
- AIPL1 Antibody - C-terminal region
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Séquence
- DLDELQKEPQ PLVFVIELLQ VDAPSDYQRE TWNLSNHEKM KAVPVLHGEG
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Homologie
- Cow: 79%, Horse: 86%, Human: 100%, Mouse: 77%, Pig: 86%, Rabbit: 79%, Rat: 77%
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Attributs du produit
- This is a rabbit polyclonal antibody against AIPL1. It was validated on Western Blot.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the C-terminal region of human AIPL1
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP72738-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- AIPL1 (Aryl Hydrocarbon Receptor Interacting Protein-Like 1 (AIPL1))
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Autre désignation
- AIPL1
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Sujet
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Background Information: Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5 % of all inherited retinal diseases. Affected individuals are diagnosed at birth or in the first few months of life with nystagmus, severely impaired vision or blindness and an abnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, is located within the LCA4 candidate region. The encoded protein contains three tetratricopeptide motifs, consistent with chaperone or nuclear transport activity. Mutations in this gene may cause approximately 20 % of recessive LCA. Alternative splicing results in multiple transcript variants.
Gene Name: aryl hydrocarbon receptor interacting protein-like 1
Alternative Symbols: LCA4, AIPL2
Protein Name: aryl-hydrocarbon-interacting protein-like 1
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Poids moléculaire
- 29kDa
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ID gène
- 23746
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NCBI Accession
- NP_001272332
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UniProt
- F1T0C4
Antigène
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