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- Validations
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- Product number
- ABIN954344 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Prune Homolog (Drosophila) (PRUNE) (AA 367-397), (C-Term) antibody
- Antibody type
- Polyclonal
- Description
- Purified through a Protein A column followed by peptide affinity purification
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 367-397, C-Term
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
Domain mapping on the human metastasis regulator protein h-Prune reveals a C-terminal dimerization domain.
Glycogen synthase kinase 3 and h-prune regulate cell migration by modulating focal adhesions.
Overexpression of h-prune in breast cancer is correlated with advanced disease status.
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activity.
Evidence for interaction between human PRUNE and nm23-H1 NDPKinase.
Vieira AR, McHenry TG, Daack-Hirsch S, Murray JC, Marazita ML
Genetics in medicine : official journal of the American College of Medical Genetics 2008 Sep;10(9):668-74
Genetics in medicine : official journal of the American College of Medical Genetics 2008 Sep;10(9):668-74
Domain mapping on the human metastasis regulator protein h-Prune reveals a C-terminal dimerization domain.
Middelhaufe S, Garzia L, Ohndorf UM, Kachholz B, Zollo M, Steegborn C
The Biochemical journal 2007 Oct 15;407(2):199-205
The Biochemical journal 2007 Oct 15;407(2):199-205
Glycogen synthase kinase 3 and h-prune regulate cell migration by modulating focal adhesions.
Kobayashi T, Hino S, Oue N, Asahara T, Zollo M, Yasui W, Kikuchi A
Molecular and cellular biology 2006 Feb;26(3):898-911
Molecular and cellular biology 2006 Feb;26(3):898-911
Overexpression of h-prune in breast cancer is correlated with advanced disease status.
Zollo M, Andrè A, Cossu A, Sini MC, D'Angelo A, Marino N, Budroni M, Tanda F, Arrigoni G, Palmieri G
Clinical cancer research : an official journal of the American Association for Cancer Research 2005 Jan 1;11(1):199-205
Clinical cancer research : an official journal of the American Association for Cancer Research 2005 Jan 1;11(1):199-205
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activity.
Forus A, D'Angelo A, Henriksen J, Merla G, Maelandsmo GM, Flørenes VA, Olivieri S, Bjerkehagen B, Meza-Zepeda LA, del Vecchio Blanco F, Müller C, Sanvito F, Kononen J, Nesland JM, Fodstad Ø, Reymond A, Kallioniemi OP, Arrigoni G, Ballabio A, Myklebost O, Zollo M
Oncogene 2001 Oct 18;20(47):6881-90
Oncogene 2001 Oct 18;20(47):6881-90
Evidence for interaction between human PRUNE and nm23-H1 NDPKinase.
Reymond A, Volorio S, Merla G, Al-Maghtheh M, Zuffardi O, Bulfone A, Ballabio A, Zollo M
Oncogene 1999 Dec 2;18(51):7244-52
Oncogene 1999 Dec 2;18(51):7244-52
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