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ITEM#: 3042-HPA020044100UL
MFR#: HPA020044-100UL
RAD21 (RAD21 homolog, S. pombe) is a novel nuclear protein located on chromosome 8q24.
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
Anti-RAD21 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
|
RAD21 (RAD21 homolog, S. pombe) is a novel nuclear protein located on chromosome 8q24. | 3042-HPA02004425UL | EA | |
Anti-WAS antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
|
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-WAS antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
|
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-DGKI antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
|
DGKI (Diacylglycerol kinase iota) is a small, integral membrane protein belonging to the type IV diacylglycerol kinase subfamily. It is mapped on chromosome 7q32.3-q33. The members of the DGK family consist of a catalytic domain and at least two cyst | 3042-HPA021924100UL | EA | |
Anti-DNAJC30 antibody produced in rabbit Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
|
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 |