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a rare genetic disorder that predisposes affected individuals to venous thrombosis and habitual abortion
DF8051-200
Background: This gene encodes a member of the Kruppel C2H2-type zinc-finger family of proteins
Immunogen: A synthesized peptide derived from human SLC41A3
corresponding to amino acids 293-342 of Human DNAM-1
Kaiso Monoclonal Antibody-MB11136 Stem Cells a rare genetic disorder thatKaiso Monoclonal Antibody Sizes: 50l, 100l Catalogue Numbers: MB11136 50, MB11136 100 Product: 50mM Tris Glycine(pH 7. 4), 0. 15M NaCl, 40% Glycerol, 0. 01% Sodium azide and 0. 05% BSA Swiss Prot: Q86T24 Host: Rabbit Reactivity: Human, Rat Applications: WB All Applications: WB: 1 500 1 1000 Background: Transcriptional regulator with bimodal DNA binding specificity. Binds to methylated CpG dinucleotides in the consensus sequence 5' CGCG 3' and also