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ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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- Product number
- HPA042567 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA042567, RRID:AB_2678055
- Product name
- Anti-TAPT1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human TAPT1, Gene description: transmembrane anterior posterior transformation 1, Alternative Gene Names: FLJ90013, Validated applications: IHC, Uniprot ID: Q6NXT6, 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
- 0.4 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
A progeroid syndrome caused by a deep intronic variant in
TAPT1
is revealed by RNA/SI‐NET sequencing
Functional characterization of the first missense variant in CEP78 , a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia
Nabavizadeh N, Bressin A, Shboul M, Moreno Traspas R, Chia P, Bonnard C, Szenker‐Ravi E, Sarıbaş B, Beillard E, Altunoglu U, Hojati Z, Drutman S, Freier S, El‐Khateeb M, Fathallah R, Casanova J, Soror W, Arafat A, Escande‐Beillard N, Mayer A, Reversade B
EMBO Molecular Medicine 2023;15(2)
EMBO Molecular Medicine 2023;15(2)
Functional characterization of the first missense variant in CEP78 , a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
Ascari G, Peelman F, Farinelli P, Rosseel T, Lambrechts N, Wunderlich K, Wagner M, Nikopoulos K, Martens P, Balikova I, Derycke L, Holtappels G, Krysko O, Van Laethem T, De Jaegere S, Guillemyn B, De Rycke R, De Bleecker J, Creytens D, Van Dorpe J, Gerris J, Bachert C, Neuhofer C, Walraedt S, Bischoff A, Pedersen L, Klopstock T, Rivolta C, Leroy B, De Baere E, Coppieters F
Human Mutation 2020;41(5):998-1011
Human Mutation 2020;41(5):998-1011
Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia
Symoens S, Barnes A, Gistelinck C, Malfait F, Guillemyn B, Steyaert W, Syx D, D’hondt S, Biervliet M, De Backer J, Witten E, Leikin S, Makareeva E, Gillessen-Kaesbach G, Huysseune A, Vleminckx K, Willaert A, De Paepe A, Marini J, Coucke P
The American Journal of Human Genetics 2015;97(4):521-534
The American Journal of Human Genetics 2015;97(4):521-534
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