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USH1C Antibody

CAT: 0223-19-353Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0223-19-353Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene.
NCBI Gene ID
564412
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of zebrafish USH1C (NP_001035018.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Apoptosis, Cell Cycle, Neuroscience
Purification
Affinity purification
Positive Control
HT-29
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: 73kDa
Fragment
IgG
Symbol
USH1C
Positive Control 2
Mouse kidney
Positive Control 3
Mouse small intestine
Positive Control 4
Rat testis
Positive Control 5
Rat kidney
NCBI Official Name
Usher syndrome 1C
NCBI Organism
Danio rerio
Other Product Names
Zgc:136806, harmonin, Usher syndrome 1C (autosomal recessive, severe), harmonin pseudogene
Tested Applications
WB, IHC
Physical Properties
Liquid

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