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Anti-KAL1卡尔曼综合征基因1抗体
点击次数：140发布时间：2012/12/26 2:41:56
更新日期：2024/9/5 14:43:27
所 在 地：其它
产品型号：BY-11053R
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货号：BY-11053R
英文名称：Anti-KAL1
中文名称：卡尔曼综合征基因1抗体
其他名称：KAL;Adhesion molecule-like X-linked;ADMLX;Anosmin-1;HHA;KAL1;KALIG 1;KALIG1;Kallmann syndrome 1 sequence （anosmin 1）;Kallmann syndrome interval gene 1;Kallmann syndrome protein;KALM;KALM_HUMAN;KMS.
抗体来源：Rabbit
克隆类型：polyclonal
蛋白分子量：predicted molecular weight: 200kDa
纯化方法：affinity purified by Protein A
交叉反应：hu
产品介绍：May be an adhesion-like molecule with anti-protease activity.Function : May be an adhesion-like molecule with anti-protease activity.Subcellular Location : Cell surface.Post-translational modifications : N-glycosylated.DISEASE : Defects in KAL1 are the cause of Kallmann syndrome type 1 （KAL1） [MIM:308700]; also known as hypogonadotropic hypogonadism ａnd anosmia. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs ａnd tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone ａnd probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In some patients other developmental anomalies can be present, which include renal agenesis, cleft lip and/or palate, selective tooth agenesis, ａnd bimanual synkinesis. In some cases anosmia may be absent or inconspicuous.Similarity : Contains 4 fibronectin type-III domains.Contains 1 WAP domain.
