Source: | Rabbit | Gene Id: | 3730 |
Isotype: | IgG | Swiss Prot: | P23352 |
purity: | Affinity purification |
Background: |
Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq |
Reactivity | Human |
Tested applications | WB |
Clonality | Polyclonal Antibody |
Calculated MW | 76 kDa |
Recommended Dilutions |
WB 1:500-1:1000
|
Immunogen | A synthetic peptide |
Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
Synonym | adhesion molecule-like X-linked, ADMLX, anosmin-1, HHA, KAL, KALIG-1, KALIG1, Kallmann syndrome 1, KALM, KMS |
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