Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA026727 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA026727, RRID:AB_1847644
- Product name
- Anti-DHDDS
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human DHDDS, Gene description: dehydrodolichyl diphosphate synthase, Alternative Gene Names: DS, FLJ13102, HDS, RP59, Validated applications: IHC, Uniprot ID: Q86SQ9, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.1 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews
Courage C, Oliver K, Park E, Cameron J, Grabińska K, Muona M, Canafoglia L, Gambardella A, Said E, Afawi Z, Baykan B, Brandt C, di Bonaventura C, Chew H, Criscuolo C, Dibbens L, Castellotti B, Riguzzi P, Labate A, Filla A, Giallonardo A, Berecki G, Jackson C, Joensuu T, Damiano J, Kivity S, Korczyn A, Palotie A, Striano P, Uccellini D, Giuliano L, Andermann E, Scheffer I, Michelucci R, Bahlo M, Franceschetti S, Sessa W, Berkovic S, Lehesjoki A
The American Journal of Human Genetics 2021;108(4):722-738
The American Journal of Human Genetics 2021;108(4):722-738
A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews
Zelinger L, Banin E, Obolensky A, Mizrahi-Meissonnier L, Beryozkin A, Bandah-Rozenfeld D, Frenkel S, Ben-Yosef T, Merin S, Schwartz S, Cideciyan A, Jacobson S, Sharon D
The American Journal of Human Genetics 2011;88(2):207-215
The American Journal of Human Genetics 2011;88(2):207-215
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