MYH9 antibody [N1-2], N-term

Eine Lieferung in diese Region ist nicht möglich.

SKU:: GTX113236
Zusätzliche Namen:: myosin heavy chain 9 , BDPLT6 , DFNA17 , EPSTS , FTNS , MATINS , MHA , NMHC-II-A , NMMHC-IIA , NMMHCA
Anwendung:: WB, IHC-P, IHC-Fr, IF, ICC, IP
Konzentration:: 0.7 mg/ml
Physischer Zustand:: Liquid
Spezies-Reaktivität:: Human
Aufreinigung:: Affinity Purified
Lagerbedingungen:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:: Genetex
Host:: Rabbit
Reaktivitäten:: Human, Mouse, Rat
Buffer:: PBS, 20% Glycerol, 0.025% ProClin 300.
Immunogen:: Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
Klon:: N1-2
Uniprot:: P35579
Synonyme:: BDPLT6;cellular myosin heavy chain, type A;DFNA17;EPSTS;FTNS;MATINS;MHA;Myosin heavy chain 9;Myosin heavy chain, non-muscle IIa;myosin-9;myosin, heavy chain 9, non-muscle;NMHC-II-A;NMMHC-IIA;NMMHCA;non-muscle myosin heavy chain 9;non-muscle myosin heavy chain A;non-muscle myosin heavy chain IIa;non-muscle myosin heavy polypeptide 9;nonmuscle myosin heavy chain II-A
Weitere Details:: This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq]

Versandbedingungen:: Blue Ice