SMPX rabbit pAb
This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011],
Product Specifications
Background
This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]
UniProt
Q9UHP9
Swiss Prot
Q9UHP9
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human SMPX AA range: 21-71
Clonality
Polyclonal
Source
Rabbit
Applications
IHC; IF
Concentration
1 mg/ml
Dilution
IHC-p 1: 50-200
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Nucleus, muscle tendon junction, integral component of membrane, M band, costamere
Gene ID (Human)
23676
Available Sizes
Frequently Asked Questions
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