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
Gene ID
23676
UniProt
Q9UHP9
Cellular Locus
Nucleus,muscle tendon junction,integral component of membrane,M band,costamere,
Host
Rabbit
Species Reactivity
Human,Mouse,Rat
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human SMPX AA range: 21-71
Clonality
Polyclonal
Isotype
IgG
Source
Rabbit
Applications
IHC, IF
Validated Applications
IHC,IF
Stability
-20°C/1 year
Concentration
1 mg/mL
Dilution
IHC-p 1: 50-200
Storage Conditions
PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES13046-1.pdf
Subcellular Location
Nucleus, muscle tendon junction, integral component of membrane, M band, costamere
Gene ID (Human)
23676
SwissProt (Human)
Q9UHP9
Available Sizes
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