Product Name	Recombinant Rabbit Anti-TMEM248 Monoclonal Antibody
Cat No.	SLA3549M
Alias	C7orf42; 0610007L01Rik; A930023A16Rik; G430067H08Rik; TM248_HUMAN; TMEM248; TM248_MOUSE; TM248_RAT; transmembrane protein 248; chromosome 7 open reading frame 42; TM248
Host Species	Rabbit
Isotype	IgG
Clonality	Monoclonal
Clone No.	5E2
React Species	Human,Mouse,Rat
Applications	WB (1:500-2000) Flow-Cyt (1:50-100) Not yet tested in other applications. Optimal working dilutions must be determined by the end user.
Purification	affinity purified by Protein A
Gene ID	55069
Swiss-Prot	Q9NWD8
Storage	0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background	Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.