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Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia
*Isoschizomers may have different methylation sensitivities
Exact LOD/LOQ should be established during laboratory validation
DNase-free
Optional tube adapters further expand compatibility with different tube sizes and laboratory vessels
SEC22B rabbit polyclonal antibody package:50 μl Mutations in this gene areSpecification Full name SEC22B rabbit polyclonal antibody Alternative names 50 l 100 l Reactivity rabbit polyclonal Applications WB, IHC Host Rabbit Clone type rabbit polyclonal Target Background The protein encoded by this gene is a member of the SEC22 family of vesicle trafficking proteins. It seems to complex with SNARE and it is thought to play a role in the ER Golgi protein trafficking. This protein has strong similarity to Mus musculus and
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