USH1C Antibody
Product Specifications
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
10083
Swiss Prot
Q9Y6N9
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 264-533 of human USH1C (NP_001284693.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Apoptosis, Cell Cycle, Neuroscience
Purification
Affinity purification
Positive Control
293T
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.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=14-505
Calculated Molecular Weight
Observed: 62kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
USH1C
Positive Control 2
HeLa
Positive Control 3
Mouse kidney
Positive Control 4
Mouse small intestine
Positive Control 5
Rat kidney
NCBI Official Name
Usher syndrome 1C (autosomal recessive, severe)
NCBI Organism
Homo sapiens
Other Product Names
USH1C, AIE-75, DFNB18, PDZ-45, PDZ-73, HARMONIN, NY-CO-37, NY-CO-38, PDZ-73/NY-CO-38, Usher syndrome 1C (autosomal recessive, severe), harmonin, PDZ-73 protein, ush1cpst, deafness, autosomal recessive 18, AIE75
Tested Applications
WB
Physical Properties
Liquid
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