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ITEM#: 3042-HPA001644100UL
MFR#: HPA001644-100UL
Anti-MYH9 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
Anti-MYH9 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
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Anti-MYH9 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution | 3042-HPA00164425UL | EA | |
Anti-WAS antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
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Wiskott-Aldrich Syndrome protein (WAS) is a hematopoietic-specific protein. It is expressed in lymphocytes, spleen, and thymus. WAS mainly is involved in the stimulation of the actin nucleation factor, Arp2/3, complex for actin polymerization and act | 3042-HPA00202225UL | EA | |
Anti-WAS antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
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Wiskott-Aldrich Syndrome protein (WAS) is a hematopoietic-specific protein. It is expressed in lymphocytes, spleen, and thymus. WAS mainly is involved in the stimulation of the actin nucleation factor, Arp2/3, complex for actin polymerization and act | 3042-HPA002022100UL | EA | |
Anti-DNAJC30 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
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DNAJC30 (DnaJ heat shock protein family (Hsp40) member C30) encodes a DNAJ-like chaperone, which may be associated with the Williams-Beuren syndrome (WBS), a developmental disorder. In WBS, deletion of contiguous genes at 7q11.23 has been reported. | 3042-HPA017318100UL | EA | |
Anti-DMPK antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
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DMPK (dystrophia myotonica protein kinase) gene is localized to human chromosome 19q13.3, which codes for a Ser/Thr kinase. This gene is localized to myotonic dystrophy (DM) locus, and belongs to the myotonic dystrophy proteinkinase family. This gene | 3042-HPA008905100UL | EA |