GLYCTK Antibody
Product Sizes
100 ul
£332.00
CSB-PA219793-100UL
About this Product
- SKU:
- CSB-PA219793
- Additional Names:
- CG9886 like antibody; GLCTK_HUMAN antibody; Glycerate kinase antibody; Glyctk antibody; GLYCTK1 antibody; HBeAg binding protein 2 antibody; HBeAg binding protein 4 antibody; HBeAg-binding protein 4 antibody; HBeAgBP4A antibody; HBEBP2 antibody; HBEBP4 antibody
- Application:
- ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
- Buffer:
- phosphate buffered saline (without mg2+ and ca2+)
- Clonality:
- Polyclonal
- Extra Details:
- Defects in GLYCTK are the cause of D-glyceric aciduria (D-GA). D-GA is a rare metabolic disease characterized by chronic metabolic acidosis and a highly variable clinical phenotype. Clinical features range from an encephalopathic presentation with seizures, microcephaly, severe mental retardation and early death, to milder manifestations with only speech delay or even normal development. Belongs to the glycerate kinase type-2 family. 7 isoforms of the human protein are produced by alternative splicing. Guo J.-H., DNA Seq. 17:1-7(2006). Wan D., Proc. Natl. Acad. Sci. U.S.A. 101:15724-15729(2004). Ota T., Nat. Genet. 36:40-45(2004).
- Host:
- Rabbit
- Immunogen:
- Synthesized peptide derived from internal of Human GLCTK.
- Isotype:
- IgG
- Physical State:
- Liquid
- Purification:
- Affinity Purified
- Reactivities:
- Human, Mouse, Rat
- Shipping Conditions:
- Blue Ice
- Storage Conditions:
- -20[o]C/-70[o]C Avoid freeze/thaw cycles.
- Supplier:
- Cusabio
- Type:
- Antibody: Polyclonal Antibody
- Manufacturer's Data Sheet:GLYCTK-Antibody-11085146.html
