SNRPN — 카탈로그 5건
Gene SNRPN
NCBI Gene 6638
취급 제조사 2곳
국내 소싱 가능
5건
mRNA Splicing - Major Pathway
Prader-Willi syndromeneurodegenerative diseaseautism spectrum disorderblood protein amountSubdural hemorrhageglutamine measurementlevel of MIT domain-containing protein 1 in blood serummuscular disease
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. · Nat Genet (1995)Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster. · Nat Genet (2008)Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. · Nat Genet (1994)
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| 견적 | 제조사 | Cat No | Mfr No | 제품명 | Host | Clonality | Reactivity | Application | Size |
|---|---|---|---|---|---|---|---|---|---|
| Biosynth | F502-117615-01 | 70R-14312 | SNRPN antibody | Rabbit | Polyclonal | Human | WB, IHC-P, ICC | 0.1 mg | |
| Biosynth | F502-123650-01 | 70R-20434 | SNRPN antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse, Rat | ELISA, IHC, IF, WB | 50 ul | |
| Biosynth | F502-139330-01 | 70R-8478 | SNRPN antibody | Rabbit | Polyclonal | Human; Cross: Predicted: Human, Mouse, Rat, Cow, Dog, Guinea Pig, Horse, Rabbit, Zebrafish | WB | 100 ul | |
| ELK Biotechnology | T376-119879-01 | ES4187 | SNRPN rabbit pAb | Rabbit | Polyclonal | Human;Mouse;Rat | WB;IHC | 50μL |