PRPF31 Antibody (PACO03815)
- SKU:
- PACO03815
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | PRPF31 Antibody |
抗体コード: | PACO03815 |
サイズ: | 50ug |
宿主種: | Rabbit |
申し込み: | ELISA, WB |
推奨される希釈: | WB:1:500-1:2000 |
反応性: | Human, Mouse |
免疫原: | synthesized peptide derived from the Internal region of human PRPF31. |
憲法: | Liquid |
ストレージバッファ: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
精製方法: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
シノニム: | PRPF31; PRP31; U4/U6 small nuclear ribonucleoprotein Prp31; Pre-mRNA-processing factor 31; Serologically defined breast cancer antigen NY-BR-99; U4/U6 snRNP 61 kDa protein; Protein 61K; hPrp31 |
UniProt Protein Function: | PRPF31: Involved in pre-mRNA splicing. Required for U4/U6.U5 tri-snRNP formation. Defects in PRPF31 are the cause of retinitis pigmentosa type 11 (RP11). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP11 inheritance is autosomal dominant. Belongs to the PRP31 family. 3 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:RNA splicing; Spliceosome; RNA-binding Chromosomal Location of Human Ortholog: 19q13.42 Cellular Component: Cajal body; nuclear speck; nucleoplasm; nucleus; U4/U6 x U5 tri-snRNP complex Molecular Function:protein binding; ribonucleoprotein binding; U4 snRNA binding; U4atac snRNA binding Biological Process: assembly of spliceosomal tri-snRNP; nuclear mRNA splicing, via spliceosome; snoRNA localization Disease: Retinitis Pigmentosa 11 |
NCBI Summary: | This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009] |
UniProt Code: | Q8WWY3 |
NCBI GenInfo Identifier: | 90101442 |
NCBI Gene ID: | 26121 |
NCBI Accession: | Q8WWY3.2 |
UniProt Secondary Accession: | Q8WWY3,Q17RB4, Q8N7F9, Q9H271, Q9Y439, E7ESA8, F1T0A4 |
UniProt Related Accession: | Q8WWY3 |
Molecular Weight: | 54,909 Da |
NCBI Full Name: | U4/U6 small nuclear ribonucleoprotein Prp31 |
NCBI Synonym Full Names: | pre-mRNA processing factor 31 |
NCBI Official Symbol: | PRPF31 |
NCBI Official Synonym Symbols: | RP11; PRP31; SNRNP61; NY-BR-99 |
NCBI Protein Information: | U4/U6 small nuclear ribonucleoprotein Prp31 |
UniProt Protein Name: | U4/U6 small nuclear ribonucleoprotein Prp31 |
UniProt Synonym Protein Names: | Pre-mRNA-processing factor 31; Serologically defined breast cancer antigen NY-BR-99; U4/U6 snRNP 61 kDa protein; Protein 61K; hPrp31 |
Protein Family: | U4/U6 small nuclear ribonucleoprotein |
UniProt Gene Name: | PRPF31 |
UniProt Entry Name: | PRP31_HUMAN |