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Cat. No.	Product Name	Species	Expression System
TMPY-02544	FANCA Protein, Human, Recombinant (His) FA-H,FA1,FAA,FAH,FANCH,FACA,Fanconi anemia, complem...	Human	Baculovirus Insect Cells
	FANCA is one of the six known Fanconi anemia gene products (FANCA, FANCC, FANCD2, FANCE, FANCF, and FANCG proteins). Fanconi anemia (FA) is a genetic disorder predisposing to aplastic anemia and cancer characterized by hypersensitivity to DNA-damaging agents and oxidative stress. FANCA associates with the IκB kinase (IKK) signalsome via interaction with IKK2. Components of the FANCA complex undergo rapid, stimulus-dependent changes in phosphorylation, which are blocked by kinase-inactive IKK2.
TMPK-00922	DLK1 Protein, Human, Recombinant (aa 24-303, His) FA1,Pref1,DLK1,pG2,DLK,secredeltin,ZOG,DLK-1	Human	HEK293 Cells
	paternally inherited genetic defects of DLK1 were identified in four families with nonsyndromic CPP and a metabolic phenotype. DLK1 encodes a transmembrane protein that is important for adipose tissue homeostasis and neurogenesis and is located in the imprinted chromosome 14q32 region associated with Temple syndrome. DLK1 Protein, Human, Recombinant (aa 24-303, His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 30.9 kDa and the accession number is P8037...
TMPJ-00876	FAH Protein, Human, Recombinant (His) Fumarylacetoacetate Hydrolase,β-Diketonase,FAH,FAA,Fumarylac...	Human	HEK293 Cells
	Fumarylacetoacetase belongs to the FAH family. Fumarylacetoacetase is primary expressed in liver and kidney. It exists as a homodimer and catalyzes the hydrolysis of 4-fumarylacetoacetate into fumarate and acetoacetate. Defects in Fumarylacetoacetase cause tyrosinemia type 1, which is congenital metabolism defect characterized by elevated levels of tyrosine in the blood and urine, and hepatorenal manifestations. Typical features include renal tubular injury, self-mutilation, hepatic necrosis, ep...
TMPK-00921	DLK1 Protein, Human, Recombinant (hFc) DLK1,FA1,pG2,ZOG,secredeltin,DLK,Pref1,DLK-1	Human	HEK293 Cells
	paternally inherited genetic defects of DLK1 were identified in four families with nonsyndromic CPP and a metabolic phenotype. DLK1 encodes a transmembrane protein that is important for adipose tissue homeostasis and neurogenesis and is located in the imprinted chromosome 14q32 region associated with Temple syndrome. DLK1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weight is 56.58 kDa and the accession number is P80370-1.

重组蛋白

FANCA Protein, Human, Recombinant (His)

Cat.No: TMPY-02544

Species: Human

Expression System: Baculovirus Insect Cells

DLK1 Protein, Human, Recombinant (aa 24-303, His)

Cat.No: TMPK-00922

Species: Human

Expression System: HEK293 Cells

FAH Protein, Human, Recombinant (His)

Cat.No: TMPJ-00876

Species: Human

Expression System: HEK293 Cells

DLK1 Protein, Human, Recombinant (hFc)

Cat.No: TMPK-00921

Species: Human

Expression System: HEK293 Cells

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