|Other Names||Anosmin-1, Adhesion molecule-like X-linked, Kallmann syndrome protein, KAL1, ADMLX, KAL, KALIG1|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.|
|Precautions||This product is for research use only. Not for use in diagnostic or therapeutic procedures.|
|Function||Has a dual branch-promoting and guidance activity, which may play an important role in the patterning of mitral and tufted cell collaterals to the olfactory cortex (By similarity). Chemoattractant for fetal olfactory epithelial cells.|
|Cellular Location||Cell membrane; Peripheral membrane protein. Secreted. Note=Proteolytic cleavage may release it from the cell surface into the extracellular space|
|Tissue Location||Expressed in the cerebellum (at protein level).|
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Provided below are standard protocols that you may find useful for product applications.
Mutations in this gene cause the X-linked Kallmannsyndrome. The encoded protein is similar in sequence to proteinsknown to function in neural cell adhesion and axonal migration. Inaddition, this cell surface protein is N-glycosylated and may haveanti-protease activity.
Dode, C., et al. Ann. Endocrinol. (Paris) 71(3):149-157(2010)Tengara, S., et al. J. Dermatol. Sci. 58(1):64-71(2010)Jian, B., et al. Cell Cycle 8(22):3770-3776(2009)Tang, K.F., et al. Asian J. Androl. 11(6):711-715(2009)Hu, Y., et al. J. Biol. Chem. 284(43):29905-29920(2009)
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