Nyctalopin anticorps (AA 282-481)
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- Antigène Voir toutes Nyctalopin (NYX) Anticorps
- Nyctalopin (NYX)
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Épitope
- AA 282-481
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Nyctalopin est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- LLYLDRNSIA FVEEGAFQNL SGLLALHLNG NRLTVLAWVA FQPGFFLGRL FLFRNPWCCD CRLEWLRDWM EGSGRVTDVP CASPGSVAGL DLSQVTFGRS SDGLCVDPEE LNLTTSSPGP SPEPAATTVS RFSSLLSKLL APRVPVEEAA NTTGGLANAS LSDSLSSRGV GGAGRQPWFL LASCLLPSVA QHVVFGLQMD
- Réactivité croisée
- Humain, Souris
- Attributs du produit
- Polyclonal Antibodies
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 282-481 of human NYX (NP_072089.1).
- Isotype
- IgG
- Top Product
- Discover our top product NYX Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:100
- Commentaires
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- Nyctalopin (NYX)
- Autre désignation
- NYX (NYX Produits)
- Synonymes
- anticorps MGC84276, anticorps CLRP, anticorps CSNB1, anticorps CSNB1A, anticorps CSNB4, anticorps NBM1, anticorps CLNP, anticorps nob, anticorps RGD1561300, anticorps nyctalopin, anticorps nyctalopin L homeolog, anticorps uncharacterized LOC491837, anticorps NYX, anticorps nyx.L, anticorps LOC491837, anticorps nyx, anticorps Nyx
- Sujet
- The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB.,NYX,CLRP,CSNB1,CSNB1A,CSNB4,NBM1,Neuroscience,NYX
- Poids moléculaire
- 52 kDa
- ID gène
- 60506
- UniProt
- Q9GZU5
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