MLXPL rabbit pAb

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MLXPL rabbit pAb

商品货号： PLA020297

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： MLXIPL BHLHD14 MIO WBSCR14
蛋白名称： MLXPL
Human_gene_id： 51085
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51085
Human_swiss_prot_no： Q9NP71
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9NP71/entry
Mouse_gene_id： 58805
Mouse_gene_link： https://www.uniprot.org/uniprot/58805
Mouse_swiss_prot_no： Q99MZ3
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q99MZ3
Rat_gene_id： 171078
Rat_gene_link： https://www.uniprot.org/uniprot/171078
Rat_swiss_prot_no： Q8VIP2
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q8VIP2
特异性： This antibody detects endogenous levels of MLXPL at Human/Mouse/Rat
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
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
分子量： 94kD
功能： disease:Haploinsufficiency of WBSCR14 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Transcriptional repressor. Binds to the canonical and non-canonical E box sequences 5'-CACGTG-3'.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Binds DNA as a heterodimer with TCFL4/MLX.,tissue specificity:Expressed in liver, heart, kidney, cerebellum and intestinal tissues.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus.
组织表达： Expressed in liver, heart, kidney, cerebellum and intestinal tissues.
科研货号： PLA020297

MLXPL rabbit pAb

Catalog No PLA020297

Product information

基因名称： MLXIPL BHLHD14 MIO WBSCR14
蛋白名称： MLXPL
Human_gene_id： 51085
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51085
Human_swiss_prot_no： Q9NP71
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9NP71/entry
Mouse_gene_id： 58805
Mouse_gene_link： https://www.uniprot.org/uniprot/58805
Mouse_swiss_prot_no： Q99MZ3
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q99MZ3
Rat_gene_id： 171078
Rat_gene_link： https://www.uniprot.org/uniprot/171078
Rat_swiss_prot_no： Q8VIP2
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q8VIP2
特异性： This antibody detects endogenous levels of MLXPL at Human/Mouse/Rat
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
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
分子量： 94kD
功能： disease:Haploinsufficiency of WBSCR14 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Transcriptional repressor. Binds to the canonical and non-canonical E box sequences 5'-CACGTG-3'.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Binds DNA as a heterodimer with TCFL4/MLX.,tissue specificity:Expressed in liver, heart, kidney, cerebellum and intestinal tissues.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus.
组织表达： Expressed in liver, heart, kidney, cerebellum and intestinal tissues.
科研货号： PLA020297

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