ABIN1706174
antibody from antibodies-online
Targeting: TP63
EEC3, KET, NBP, OFC8, p51, p53CP, p63, p73H, p73L, SHFM4, TP53CP, TP53L, TP73L
Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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- Product number
- ABIN1706174 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Tumor Protein P63 (TP63) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide corresponding to a sequence at the C-terminal of human PROM1, different from the related rat sequence by two amino acids, and from the related mouse sequence by three amino acids.Immunogen affinity purified.
- Reactivity
- Human, Rat
- Host
- Rabbit
- Epitope
- C-Term
- Isotype
- IgG
- Vial size
- 100 μg
- Storage
- At -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
Identification of a cancer stem cell in human brain tumors.
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
Torrente Y, Belicchi M, Sampaolesi M, Pisati F, Meregalli M, D'Antona G, Tonlorenzi R, Porretti L, Gavina M, Mamchaoui K, Pellegrino MA, Furling D, Mouly V, Butler-Browne GS, Bottinelli R, Cossu G, Bresolin N
The Journal of clinical investigation 2004 Jul;114(2):182-95
The Journal of clinical investigation 2004 Jul;114(2):182-95
Identification of a cancer stem cell in human brain tumors.
Singh SK, Clarke ID, Terasaki M, Bonn VE, Hawkins C, Squire J, Dirks PB
Cancer research 2003 Sep 15;63(18):5821-8
Cancer research 2003 Sep 15;63(18):5821-8
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
Maw MA, Corbeil D, Koch J, Hellwig A, Wilson-Wheeler JC, Bridges RJ, Kumaramanickavel G, John S, Nancarrow D, Röper K, Weigmann A, Huttner WB, Denton MJ
Human molecular genetics 2000 Jan 1;9(1):27-34
Human molecular genetics 2000 Jan 1;9(1):27-34
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