×
For best experience we recommend to activate Javascript in your browser.
Nyctalopin antibody (Middle Region)
NYX
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Nyctalopin Antibody
(hide)
Target
See all Nyctalopin (NYX) Antibodies
Nyctalopin (NYX)
Binding Specificity
All epitopes for Nyctalopin antibodies
Middle Region
Reactivity
All reactivities for Nyctalopin antibodies
Human
Host
All hosts for Nyctalopin antibodies
Rabbit
Clonality
All clonalities for Nyctalopin antibodies
Polyclonal
Conjugate
All conjugates for Nyctalopin antibodies
This Nyctalopin antibody is un-conjugated
Application
All applications for Nyctalopin antibodies
Western Blotting (WB)
Sequence
GSGRVTDVPC ASPGSVAGLD LSQVTFGRSS DGLCVDPEEL NLTTSSPGPS
Purification
Affinity purified
Immunogen
The immunogen is a synthetic peptide directed towards the middle region of human NYX
Top Product
Discover our top product NYX Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
(hide)
Format
Liquid
Buffer
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 23 % sucrose.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Target Details for Nyctalopin
(hide)
Target
Nyctalopin (NYX)
Alternative Name
NYX (NYX Products )
Synonyms
MGC84276 antibody, CLRP antibody, CSNB1 antibody, CSNB1A antibody, CSNB4 antibody, NBM1 antibody, CLNP antibody, nob antibody, RGD1561300 antibody, nyctalopin antibody, nyctalopin L homeolog antibody, uncharacterized LOC491837 antibody, NYX antibody, nyx.L antibody, LOC491837 antibody, nyx antibody, Nyx antibody
Background
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. Alias Symbols: CLRP, NBM1, CSNB1, CSNB4, CSNB1A Protein Size: 481
Gene ID
60506
NCBI Accession
NM_022567 , NP_072089
UniProt
Q9GZU5
Recently viewed
(hide)