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- Antibody Data
- Antigen structure
- References [5]
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- Product number
- ABIN393591 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Retinoic Acid Receptor, alpha (RARA) (AA 1-463) antibody
- Antibody type
- Monoclonal
- Description
- This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 1-463
- Isotype
- IgG
- Antibody clone number
- S1
- Vial size
- 100 μg
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Submitted references Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.
A unique secondary-structure switch controls constitutive gene repression by retinoic acid receptor.
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
Analysis of t(15;17) chromosomal breakpoint sequences in therapy-related versus de novo acute promyelocytic leukemia: association of DNA breaks with specific DNA motifs at PML and RARA loci.
Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S, DREAM investigators.
Diabetes care 2010 Oct;33(10):2250-3
Diabetes care 2010 Oct;33(10):2250-3
MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.
Jagomägi T, Nikopensius T, Krjutskov K, Tammekivi V, Viltrop T, Saag M, Metspalu A
European journal of oral sciences 2010 Jun;118(3):213-20
European journal of oral sciences 2010 Jun;118(3):213-20
A unique secondary-structure switch controls constitutive gene repression by retinoic acid receptor.
le Maire A, Teyssier C, Erb C, Grimaldi M, Alvarez S, de Lera AR, Balaguer P, Gronemeyer H, Royer CA, Germain P, Bourguet W
Nature structural & molecular biology 2010 Jul;17(7):801-7
Nature structural & molecular biology 2010 Jul;17(7):801-7
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC
PloS one 2010 Jul 9;5(7):e11493
PloS one 2010 Jul 9;5(7):e11493
Analysis of t(15;17) chromosomal breakpoint sequences in therapy-related versus de novo acute promyelocytic leukemia: association of DNA breaks with specific DNA motifs at PML and RARA loci.
Hasan SK, Ottone T, Schlenk RF, Xiao Y, Wiemels JL, Mitra ME, Bernasconi P, Di Raimondo F, Stanghellini MT, Marco P, Mays AN, Döhner H, Sanz MA, Amadori S, Grimwade D, Lo-Coco F
Genes, chromosomes & cancer 2010 Aug;49(8):726-32
Genes, chromosomes & cancer 2010 Aug;49(8):726-32
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Supportive validation
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