DYX1C1 Antibody
Product Specifications
Background
DYX1C1contains 1 CS domain and 3 TPR repeats. A chromosomal aberration, translocation t (2;15) (q11; q21), involving DYX1C1 may be a cause of dyslexia.
NCBI Gene ID
161582
Swiss Prot
Q8WXU2
Accession Number
NP_570722
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DYX1C1.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer
Purification
Antibody is purified by peptide affinity chromatography method.
Positive Control
Cat. No. 1201 - HeLa Cell Lysate
Concentration
Batch dependent
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store DYX1C1 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Calculated Molecular Weight
48 kDa
Applications Notes
DYX1C1 antibody can be used for detection of DYX1C1 by ELISA at 1:312500. DYX1C1 antibody can be used for detection of DYX1C1 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Symbol
DYX1C1
NCBI Official Name
Dyslexia susceptibility 1 candidate 1
NCBI Organism
Homo sapiens
Background Reference 01
Marino, C., (2007) Genes Brain Behav. 6 (7), 640-646.
Other Product Names
DYX1C1, DYX1, DYXC1, EKN1, FLJ37882, MGC70618, RD, CILD25
Tested Applications
ELISA, WB
Protein ID
75677570
Physical Properties
Liquid
Curated Selection
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