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- Product number
- ABIN396823 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Coagulation Factor XIII, A1 Polypeptide (F13A1) (AA 1-733) 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 1-733
- Isotype
- IgG
- Antibody clone number
- M1
- 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 Allele-allele interaction within the F13A1 gene: a risk factor for ischaemic heart disease in Spanish population.
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).
Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders.
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
Carreras-Torres R, Athanasiadis G, Via M, Trenchs J, Gayà-Vidal M, Santamaria J, Esteban E, Moral P
Thrombosis research 2010 Sep;126(3):e241-5
Thrombosis research 2010 Sep;126(3):e241-5
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
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
A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).
Romero R, Friel LA, Velez Edwards DR, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Erez O, Chaiworapongsa T, Pearce BD, Bartlett J, Salisbury BA, Anant MK, Vovis GF, Lee MS, Gomez R, Behnke E, Oyarzun E, Tromp G, Williams SM, Menon R
American journal of obstetrics and gynecology 2010 Oct;203(4):361.e1-361.e30
American journal of obstetrics and gynecology 2010 Oct;203(4):361.e1-361.e30
Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders.
Antón AI, González-Conejero R, Roldán V, Quiroga T, Sánchez-Vega B, Corral J, Vicente V, Mezzano D
Annals of hematology 2010 Nov;89(11):1147-54
Annals of hematology 2010 Nov;89(11):1147-54
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
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