| Description | Product Introductionrecombinant, expressed in rice, suitable for cell culture, low endotoxin;It is a kind of recombinant human albumin (RHA) without animal origin. It is designed for cell culture applications and is a powerful medium supplement with superior performance to human albumin, bovine Product Introductionrecombinant, expressed in rice, suitable for cell culture, low endotoxin;It is a kind of recombinant human albumin (RHA) without animal origin. It is designed for cell culture applications and is a powerful medium supplement with superior performance to human albumin, bovine serum albumin and recombinant human albumin from other sources.It brings stable and consistent performance rather than variables related to hydrolysates and extracts. It is an ideal medium for Chinese hamster ovary (CHO), hybridoma, Vero, stem cell and primary cell culture medium.The recombinant variant is recommended for absorption, transport, metabolism and excretion (ADME) pharmacology; cell culture; drug delivery; and cell cryopreservation... Read More | Inquire | Inquire | Inquire | Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue Staining.Description:HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue Staining.Description:HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. It may also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. HSPD1 gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13). Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4); also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. HSPD1 is clinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurs within the first two decades of life... Read More |