NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience

protein

Human OFD1 (aa 551-632) Control Fragment Recombinant Protein

RP-95179

100 uL

US 259.00

Human OFD1 (aa 551-632) Control Fragment Recombinant Protein

RP-95179

100 uL

US 259.00

Recombinant

purified

Human

Blocking Assay: Assay-dependent, Control: Assay-dependent

Human

-20 C, Avoid Freeze/Thaw Cycles

This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome.

Liquid

Blocking Assay: Assay-dependent, Control: Assay-dependent

71-7A; CXorf5; DXGgc7e; JBTS10; Ofd1; OFD1 centriole and centriolar satellite protein; ofd1 protein; OFD1, centriole and centriolar satellite protein; oral-facial-digital syndrome 1; oral-facial-digital syndrome 1 gene homolog; oral-facial-digital syndrome 1 gene homolog (human); oral-facial-digital syndrome 1 protein; Oral-facial-digital syndrome 1 protein homolog; ORF2; Protein 71-7A; putative oral-facial-digital syndrome 1 protein; RGD1562231; RP23; SGBS2; wu:fa07a10; wu:fd17e11; zgc:92562