SMAL1 rabbit pAb
The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008],
Product Specifications
Background
UniProt
Q9NZC9
Swiss Prot
Q9NZC9
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human SMAL1 AA range: 485-535
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Molecular Weight
105kD
Storage Conditions
-20°C/1 year
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES13062-1.pdf
Observed Molecular Weight
105kD
Fragment
IgG
Subcellular Location
Nucleus . Recruited to damaged DNA regions.
Other Product Names
Gene ID (Human)
50485
Available Sizes
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