FZD9 Antibody
Product Specifications
Background
Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.
NCBI Gene ID
8326
Swiss Prot
O00144
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 469-591 of human FZD9 (NP_003499.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cell Cycle, Immunology, Neuroscience, Signal Transduction, Stem Cell
Purification
Affinity purification
Positive Control
TE-1
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 80kDa
Fragment
IgG
Symbol
FZD9
Positive Control 2
293T
Positive Control 3
HepG2
Positive Control 4
THP-1
Positive Control 5
U-251MG
Positive Control 6
Mouse heart
NCBI Official Name
Frizzled class receptor 9
NCBI Organism
Homo sapiens
Other Product Names
FZD9, FZD3, CD349
Tested Applications
WB, IF
Physical Properties
Liquid
Curated Selection
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