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PRPF8 Recombinant monoclonal antibody, PBS Only

PRPF8 Uni-rAb® Recombinant Antibody for WB, Indirect ELISA

Cat No. 87982-1-PBS
Clone No.260212F12

Host / Isotype

Rabbit / IgG

Reactivity

human, rat

Applications

WB, Indirect ELISA

220 kDa U5 snRNP-specific protein, HPRP8, p220, Pre-mRNA-processing-splicing factor 8, PRP8

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

87982-1-PBS targets PRPF8 in WB, Indirect ELISA applications and shows reactivity with human, rat samples.

Tested Reactivity human, rat
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

CatNo: Ag1652

Product name: Recombinant human PRPF8 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 2037-2335 aa of BC064370

Sequence: SQLTATQTRTVNKHGDEIITSTTSNYETQTFSSKTEWRVRAISAANLHLRTNHIYVSSDDIKETGYTYILPKNVLKKFICISDLRAQIAGYLYGVSPPDNPQVKEIRCIVMVPQWGTHQTVHLPGQLPQHEYLKEMEPLGWIHTQPNESPQLSPQDVTTHAKIMADNPSWDGEKTIIITCSFTPGSCTLTAYKLTPSGYEWGRQNTDKGNNPKGYLPSHYERVQMLLSDRFLGFFMVPAQSSWNYNFMGVRHDPNMKYELQLANPKEFYHEVHRPSHFLNFALLQEGEVYSADREDLYA

Predict reactive species
Full Name PRP8 pre-mRNA processing factor 8 homolog (S. cerevisiae)
Calculated Molecular Weight 274 kDa
Observed Molecular Weight~250 kDa
GenBank Accession NumberBC064370
Gene Symbol PRPF8
Gene ID (NCBI) 10594
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDQ6P2Q9
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

Pre-mRNA processing factor 8 (PRPF8) is a highly conserved core component of the spliceosome, the ribonucleoprotein complex responsible for pre-mRNA splicing in eukaryotic cells. PRPF8 is one of the largest and most central proteins within the U5 small nuclear ribonucleoprotein (snRNP) and plays a pivotal role in coordinating the catalytic steps of intron removal and exon ligation. It directly interacts with pre-mRNA, small nuclear RNAs (snRNAs), and multiple splicing factors, acting as a structural and functional scaffold for spliceosome assembly and activity. PRPF8 is ubiquitously expressed across tissues due to its essential role in gene expression. Mutations in PRPF8 have been strongly associated with retinitis pigmentosa (RP13), a degenerative retinal disease, highlighting its importance in tissue-specific splicing regulation. Additionally, altered PRPF8 function has been implicated in cancer, myelodysplastic syndromes, and other splicing-related disorders. As a key regulator of RNA processing, PRPF8 is central to transcriptome integrity and cellular homeostasis.

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