SKU: WP2009 Categories: ,

FA58A Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP2009-100
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Product details

Background:

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008],

Specifications

Size50μL/100μL
TargetFA58A
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)27kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; ELISA 1:5000-20000
FormulationLiquid in PBS containing 50% glycerol,0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human protein . at AA range: 30-110
SpecificityFA58A Polyclonal Antibody detects endogenous levels of protein.
Gene NameFAM58A
Protein NameCyclin-related protein FAM58A (Cyclin-M)
Other Name
SpeciesHuman
Gene ID92002
UniprotQ8N1B3,
Species.1Mouse
Gene ID.1
Uniprot.1Q8QZR8,
Species.2Rat
Gene ID.2
Uniprot.2Q4QQW5
Cellular Localizationcyclin-dependent protein kinase holoenzyme complex,nucleus,
Tissue ExpressionB-cell,Blood,Kidney,Lung,
Signaling_pathway
Research Areas
FunctionDisease:Defects in FAM58A are the cause of toe syndactyly, telecanthus, and anogenital and renal malformations (STAR) [MIM:300707]; also known as STAR syndrome or syndactyly with renal and anogenital malformations.,Function:May have a role in cell proliferation.,similarity:Belongs to the cyclin family. Cyclin-like FAM58 subfamily.,subunit:Interacts with SALL1.,
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