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FAM149B1 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA558687
Additional Details : Weight : 0.02000kg
Description
Immunogen sequence: ERDSTIFGIR GKKLHFSSSY AHKASSIAKS SSFCSMERDE EDSIIVSEGI IEEYLAFDHI DIEEG Highest antigen sequence identity to the following orthologs: Mouse - 68%, Rat - 71%.
Involved in cilium assembly and protein localization to cilium. Predicted to be located in cilium. Implicated in Joubert syndrome. FAM149B1 (Family With Sequence Similarity 149 Member B1) is a Protein Coding gene. Diseases associated with FAM149B1 include Joubert Syndrome 36 and Orofaciodigital Syndrome Vi. An important paralog of this gene is FAM149A. Involved in the localization of proteins to the cilium and cilium assembly. Indirectly regulates the signaling functions of the cilium, being required for normal SHH/smoothened signaling and proper development.Specifications
FAM149B1 | |
Polyclonal | |
Unconjugated | |
FAM149B1 | |
FAM149B1; family with sequence similarity 149 member B1; family with sequence similarity 149, member B1; KIAA0974; Protein FAM149B1; RGD1359592 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
317662 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry, Western Blot | |
0.1 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
Q96BN6 | |
FAM149B1 | |
Recombinant protein corresponding to Human FAM149B1 | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Research Use Only