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Kallmann syndrome 1 sequence, Mouse, Polyclonal Antibody, Abnova™
Shop All Abnova Corporation ProductsDescription
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
Specifications
Specifications
| Antigen | Kallmann syndrome 1 sequence |
| Applications | ELISA, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a partial recombinant KAL1. |
| Formulation | 50% glycerol |
| Gene | KAL1 |
| Gene Accession No. | NM_000216 |
| Gene Alias | ADMLX/HHA/KAL/KALIG-1/KMS |
| Gene Symbols | KAL1 |
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