SKU: WP7540 Categories: ,

RBM7 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP7540-100
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Product details

Background:

Specifications

Size50μL/100μL
TargetRBM7
ReactivityHuman, Mouse
ApplicationsWB
MW(Calculated)29kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
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 RBM7
SpecificityThis antibody detects endogenous levels of RBM7 at Human, Mouse
Gene NameRBM7
Protein NameRNA-binding protein 7 (RNA-binding motif protein 7)
Other Name
SpeciesHuman
Gene ID10179
UniprotQ9Y580,
Species.1Mouse
Gene ID.167010
Uniprot.1Q9CQT2
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationNucleus, nucleoplasm . Nucleus . Excluded from the nucleolus. .
Tissue ExpressionUbiquitous.
Signaling_pathway
Research Areas
FunctionRNA-binding subunit of the trimeric nuclear exosome targeting (NEXT) complex, a complex that functions as an RNA exosome cofactor that directs a subset of non-coding short-lived RNAs for exosomal degradation . NEXT is involved in surveillance and turnover of aberrant transcripts and non-coding RNAs . Binds preferentially polyuridine sequences and associates with newly synthesized RNAs, including pre-mRNAs and short-lived exosome substrates such as promoter upstream transcripts (PROMPTs), enhancer RNAs (eRNAs), and 3'-extended products from small nuclear RNAs (snRNAs) . Participates in several biological processes including DNA damage response (DDR) and stress response . During stress response, activation of the p38MAPK-MK2 pathway decreases RBM7-RNA-binding and subsequently the RNA exosome degradation activities, thereby modulating the turnover of non-coding transcriptome . Participates in DNA damage response (DDR), through its interaction with MEPCE and LARP7, the core subunits of 7SK snRNP complex, that release the positive transcription elongation factor b (P-TEFb) complex from the 7SK snRNP. In turn, activation of P-TEFb complex induces the transcription of P-TEFb-dependent DDR genes to promote cell viability .
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