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Mutations in this gene are associated with osteogenesis imperfecta types I-IV
also known as coenzyme Q
RRID: AB_2838990
DF4957-200
Background: The protein encoded by this gene belongs to the immunoglobulin superfamily
SMC1A Monoclonal Antibody-MB66490 Nucleic Acid Tranfection Mutations in this gene areSMC1A Monoclonal Antibody Sizes: 50l, 100l Catalogue Numbers: MB66490 50, MB66490 100 Product: Liquid in PBS containing 50% glycerol, 0. 5% BSA and 0. 02% sodium azide, pH 7. 3. Swiss Prot: Q14683 Host: Mouse Reactivity: Human Applications: WB, IF ICC All Applications: WB (1 500 1 1000), IF ICC (1 50 1 100) Background: Structural maintenance of chromosomes 1 (SMC1) protein is a chromosomal protein member of the cohesin complex that enables sister
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