Product description
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein .Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.Belongs to the class I fructose-bisphosphate aldolase family.
Specifications
Applications
IHC, WB, ELISA
Host
Rabbit
Clonality
Polyclonal
Isotype
IgG
Supplier
CusaBio
Shipping & storage
Shipping condition
Blue Ice
Storage temperature
-20°C

Order your product by email

Productname

ALDOA Antibody

CSB-PA00015A0Rb-100

By filling out this form, you are placing an order by e-mail. You will receive an order confirmation within one working day. The order cannot be modified after receipt of the order confirmation.


Request a sample

Productname

ALDOA Antibody

CSB-PA00015A0Rb-100

By filling out this form, you request a sample. You will receive an order confirmation within one working day. The order cannot be modified after receipt of the order confirmation.


Organization information

*Required fields


Are you looking for specific products, alternatives or documentation?