SLC17A5 — 카탈로그 4건
Gene SLC17A5
NCBI Gene 26503
취급 제조사 3곳
국내 소싱 가능
4건
Defective SLC17A5 causes Salla disease (SD) and ISSDHyaluronan degradationOrganic anion transport by SLC5/17/25 transportersSialic acid metabolism
free sialic acid storage disease, infantile formSalla diseaseneurodegenerative diseaseintermediate severe Salla diseasefree sialic acid storage diseasegenetic disorderlysosomal storage diseasehydrops fetalis
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. · Brain (2017)Molecular autopsy in maternal-fetal medicine. · Genet Med (2018)The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation. · Am J Hum Genet (2000)
체크박스로 여러 제품을 선택해 한 번에 견적을 요청하세요. 제조사·Cat No·Application을 한 표에서 비교합니다.
| 견적 | 제조사 | Cat No | Mfr No | 제품명 | Host | Clonality | Reactivity | Application | Size |
|---|---|---|---|---|---|---|---|---|---|
| Elabscience | T619-101360-01 | E-AB-91152 | SLC17A5 Polyclonal Antibody(E-AB-91152) | Rabbit | Polyclonal | Mouse, Rat | WB | 200μL | |
| Biosynth | F502-123507-01 | 70R-20304 | SLC17A5 antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse, Rat | ELISA, WB | 50 ul | |
| MyBioSource | R247-200152-01 | MBS9135411 | SLC17A5, Polyclonal Antibody | Rabbit | Polyclonal | Human, Rat | WB | ||
| Biosynth | F502-137863-01 | 70R-6694 | SLC17A5 antibody | Rabbit | Polyclonal | Human,Mouse,Rat | WB, IHC | 100 ul |