Pay in 4 interest-free payments of $69.83 Learn more
Ships within 48 hours · Estimated delivery Jul 28 - Aug 2
Defects in FGFR1 are a cause of Pfeiffer syndrome ，idiopathic hypogonadotropic hypogonadism， Kallmann syndrome type 2
Swiss-Prot: O14980(Human) Q6P5F9(Mouse) Q80U96(Rat)
BS77386-100
p53-induced gene 1 protein
SLC22A17 Antibody
FAAH2 Polyclonal Antibody - E-AB-11206 Size:200μL Defects in FGFR1 are aFAAH2 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 11206 60, E AB 11206 120, E AB 11206 200 Citations, Manuals and MSDS Available upon request. Abbreviation: FAAH2 Target Synonym: AMDD; amidase domain containing; amidase domain containing protein; Amidase domain containing protein; Anandamide amidohydrolase 2; FAAH 2; FAAH2; FAAH2; fatty acid amide hydrolase 2; Fatty acid amide hydrolase 2; FLJ31204; Oleamide hydrolase 2; RP11