Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA039751 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA039751, RRID:AB_10794754
- Product name
- Anti-OSGEP
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human OSGEP, Gene description: O-sialoglycoprotein endopeptidase, Alternative Gene Names: GCPL1, KAE1, OSGEP1, PRSMG1, Validated applications: ICC, IHC, WB, Uniprot ID: Q9NPF4, 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
- 0.05 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 Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Arrondel C, Missoury S, Snoek R, Patat J, Menara G, Collinet B, Liger D, Durand D, Gribouval O, Boyer O, Buscara L, Martin G, Machuca E, Nevo F, Lescop E, Braun D, Boschat A, Sanquer S, Guerrera I, Revy P, Parisot M, Masson C, Boddaert N, Charbit M, Decramer S, Novo R, Macher M, Ranchin B, Bacchetta J, Laurent A, Collardeau-Frachon S, van Eerde A, Hildebrandt F, Magen D, Antignac C, van Tilbeurgh H, Mollet G
Nature Communications 2019;10(1)
Nature Communications 2019;10(1)
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Braun D, Rao J, Mollet G, Schapiro D, Daugeron M, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt J, Lawson J, Schanze D, Ashraf S, Ullmann J, Hoogstraten C, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera I, Sanchez-Ferras O, Hu J, Boschat A, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee H, Choi W, Sadowski C, Pabst W, Warejko J, Daga A, Basta T, Matejas V, Scharmann K, Kienast S, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng G, Lin S, Chang J, Chen C, Cho M, Gaffney P, Gipson P, Hsu C, Kari J, Ke Y, Kiraly-Borri C, Lai W, Lemyre E, Littlejohn R, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder E, Rump P, Schnur R, Shiihara T, Sinha M, Soliman N, Soulami K, Sweetser D, Tsai W, Tsai J, Topaloglu R, Vester U, Viskochil D, Vatanavicharn N, Waxler J, Wierenga K, Wolf M, Wong S, Leidel S, Truglio G, Dedon P, Poduri A, Mane S, Lifton R, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F
Nature Genetics 2017;49(10):1529-1538
Nature Genetics 2017;49(10):1529-1538
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