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  1. Alles ansehen
  2. Polyclonal

GTX55718

MYH9 antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX55718
Zusätzliche Namen:
myosin heavy chain 9 , BDPLT6 , DFNA17 , EPSTS , FTNS , MATINS , MHA , NMHC-II-A , NMMHC-IIA , NMMHCA
Anwendung:
WB, IHC-P, IP
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
Buffer:
PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 1711-1960 of human MYH9 (NP_002464.1).
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 conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with 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, Dec 2011]
Versandbedingungen:
Blue Ice