Contactin 4 Polyclonal Antibody

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商品货号： PLA015390

适应性： 人,小鼠,大鼠

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： CNTN4
蛋白名称： Contactin-4
Human_gene_id： 152330
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=152330
Human_swiss_prot_no： Q8IWV2
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q8IWV2/entry
Mouse_gene_id： 269784
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=269784
Mouse_swiss_prot_no： Q69Z26
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q69Z26
Rat_gene_id： 116658
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=116658
Rat_swiss_prot_no： Q62845
Rat_swiss_link： http://www.uniprot.org/uniprot/Q62845
特异性： Contactin 4 Polyclonal Antibody detects endogenous levels of Contactin 4 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： CNTN4; Contactin-4; Brain-derived immunoglobulin superfamily protein 2; BIG-2
分子量： 113kD
功能： disease:A chromosomal aberration disrupting CNTN4 has been found in a boy with characteristic physical features of 3p deletion syndrome (3PDS). Translocation t(3;10)(p26;q26). 3PDS is a rare contiguous gene disorder involving the loss of the telomeric portion of the short arm of chromosome 3 and characterized by developmental delay, growth retardation, and dysmorphic features.,function:Contactins mediate cell surface interactions during nervous system development. Has some neurite outgrowth-promoting activity. May be involved in synaptogenesis.,induction:By retinoic acid, suggesting that it may act in response to differentiating agents.,similarity:Belongs to the immunoglobulin superfamily. Contactin family.,similarity:Contains 4 fibronectin type-III domains.,similarity:Contains 6 Ig-like C2-type (immunoglobulin-like) domains.,tissue specificity:Mainly expressed in brain. Highly expressed in cerebellum and weakly expressed in corpus callosum, caudate nucleus, amygdala and spinal cord. Also expressed in testis, pancreas, thyroid, uterus, small intestine and kidney. Not expressed in skeletal muscle. Isoform 2 is weakly expressed in cerebral cortex.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cell membrane; Lipid-anchor, GPI-anchor. Secreted .
组织表达： Mainly expressed in brain. Highly expressed in cerebellum and weakly expressed in corpus callosum, caudate nucleus, amygdala and spinal cord. Also expressed in testis, pancreas, thyroid, uterus, small intestine and kidney. Not expressed in skeletal muscle. Isoform 2 is weakly expressed in cerebral cortex.
科研货号： PLA015390

Contactin 4 Polyclonal Antibody

Catalog No PLA015390

Product information

基因名称： CNTN4
蛋白名称： Contactin-4
Human_gene_id： 152330
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=152330
Human_swiss_prot_no： Q8IWV2
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q8IWV2/entry
Mouse_gene_id： 269784
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=269784
Mouse_swiss_prot_no： Q69Z26
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q69Z26
Rat_gene_id： 116658
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=116658
Rat_swiss_prot_no： Q62845
Rat_swiss_link： http://www.uniprot.org/uniprot/Q62845
特异性： Contactin 4 Polyclonal Antibody detects endogenous levels of Contactin 4 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： CNTN4; Contactin-4; Brain-derived immunoglobulin superfamily protein 2; BIG-2
分子量： 113kD
功能： disease:A chromosomal aberration disrupting CNTN4 has been found in a boy with characteristic physical features of 3p deletion syndrome (3PDS). Translocation t(3;10)(p26;q26). 3PDS is a rare contiguous gene disorder involving the loss of the telomeric portion of the short arm of chromosome 3 and characterized by developmental delay, growth retardation, and dysmorphic features.,function:Contactins mediate cell surface interactions during nervous system development. Has some neurite outgrowth-promoting activity. May be involved in synaptogenesis.,induction:By retinoic acid, suggesting that it may act in response to differentiating agents.,similarity:Belongs to the immunoglobulin superfamily. Contactin family.,similarity:Contains 4 fibronectin type-III domains.,similarity:Contains 6 Ig-like C2-type (immunoglobulin-like) domains.,tissue specificity:Mainly expressed in brain. Highly expressed in cerebellum and weakly expressed in corpus callosum, caudate nucleus, amygdala and spinal cord. Also expressed in testis, pancreas, thyroid, uterus, small intestine and kidney. Not expressed in skeletal muscle. Isoform 2 is weakly expressed in cerebral cortex.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cell membrane; Lipid-anchor, GPI-anchor. Secreted .
组织表达： Mainly expressed in brain. Highly expressed in cerebellum and weakly expressed in corpus callosum, caudate nucleus, amygdala and spinal cord. Also expressed in testis, pancreas, thyroid, uterus, small intestine and kidney. Not expressed in skeletal muscle. Isoform 2 is weakly expressed in cerebral cortex.
科研货号： PLA015390

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