購物車
幫助
021-54845833/15800441009
反應種屬： Human
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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. |
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Applications: |
WB |
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Name of antibody: |
KAL1 |
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Immunogen: |
Synthesized peptide derived from internal of human KAL1. |
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Full name: |
Kallmann syndrome 1 sequence |
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Synonyms： |
HH1; HHA; KAL; KMS; ADMLX; WFDC19; KALIG-1 |
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SwissProt: |
P23352 |
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WB Predicted band size: |
76 kDa |
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WB Positive control: |
Huvec cells lysate |
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WB Recommended dilution: |
500-3000 |
