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SNAI2 rabbit pAb
商品货号: PLA021440
适 应 性: 人,小鼠,大鼠
WB IHC ELISA
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: SNAI2 SLUG SLUGH
  • 蛋白名称: SNAI2
  • Human_gene_id: 6591
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6591
  • Human_swiss_prot_no: O43623
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O43623/entry
  • Mouse_gene_id: 20583
  • Mouse_gene_link: https://www.uniprot.org/uniprot/20583
  • Mouse_swiss_prot_no: P97469
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P97469
  • Rat_gene_id: 25554
  • Rat_gene_link: https://www.uniprot.org/uniprot/25554
  • Rat_swiss_prot_no: O08954
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/O08954
  • 特异性: This antibody detects endogenous levels of Human,Mouse,Rat SNAI2
  • 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
  • 其他名称: Zinc finger protein SNAI2 (Neural crest transcription factor Slug;Protein snail homolog 2)
  • 分子量: 29kD
  • 功能: disease:Defects in SNAI2 are a cause of neural tube defects (NTD).,disease:Defects in SNAI2 are the cause of Waardenburg syndrome type 2D (WS2D) [MIM:608890]. WS2 is a genetically heterogeneous, autosomal dominant disorder characterized by sensorineural deafness, pigmentary disturbances, and absence of dystopia canthorum. The frequency of deafness is higher in WS2 than in WS1.,function:Transcriptional repressor. Involved in the generation and migration of neural crest cells.,similarity:Belongs to the snail C2H2-type zinc-finger protein family.,similarity:Contains 5 C2H2-type zinc fingers.,tissue specificity:Expressed in placenta and adult heart, pancreas, liver, kidney and skeletal muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3505
  • 细胞定位: Nucleus . Cytoplasm. Observed in discrete foci in interphase nuclei. These nuclear foci do not overlap with the nucleoli, the SP100 and the HP1 heterochromatin or the coiled body, suggesting SNAI2 is associated with active transcription or active splicing regions.
  • 组织表达: Expressed in most adult human tissues, including spleen, thymus, prostate, testis, ovary, small intestine, colon, heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Not detected in peripheral blood leukocyte. Expressed in the dermis and in all layers of the epidermis, with high levels of expression in the basal layers (at protein level). Expressed in osteoblasts (at protein level). Expressed in mesenchymal stem cells (at protein level). Expressed in breast tumor cells (at protein level).
  • 科研货号: PLA021440
SNAI2 rabbit pAb
Catalog No PLA021440
Product information
  • 基因名称: SNAI2 SLUG SLUGH
  • 蛋白名称: SNAI2
  • Human_gene_id: 6591
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6591
  • Human_swiss_prot_no: O43623
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O43623/entry
  • Mouse_gene_id: 20583
  • Mouse_gene_link: https://www.uniprot.org/uniprot/20583
  • Mouse_swiss_prot_no: P97469
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P97469
  • Rat_gene_id: 25554
  • Rat_gene_link: https://www.uniprot.org/uniprot/25554
  • Rat_swiss_prot_no: O08954
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/O08954
  • 特异性: This antibody detects endogenous levels of Human,Mouse,Rat SNAI2
  • 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
  • 其他名称: Zinc finger protein SNAI2 (Neural crest transcription factor Slug;Protein snail homolog 2)
  • 分子量: 29kD
  • 功能: disease:Defects in SNAI2 are a cause of neural tube defects (NTD).,disease:Defects in SNAI2 are the cause of Waardenburg syndrome type 2D (WS2D) [MIM:608890]. WS2 is a genetically heterogeneous, autosomal dominant disorder characterized by sensorineural deafness, pigmentary disturbances, and absence of dystopia canthorum. The frequency of deafness is higher in WS2 than in WS1.,function:Transcriptional repressor. Involved in the generation and migration of neural crest cells.,similarity:Belongs to the snail C2H2-type zinc-finger protein family.,similarity:Contains 5 C2H2-type zinc fingers.,tissue specificity:Expressed in placenta and adult heart, pancreas, liver, kidney and skeletal muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3505
  • 细胞定位: Nucleus . Cytoplasm. Observed in discrete foci in interphase nuclei. These nuclear foci do not overlap with the nucleoli, the SP100 and the HP1 heterochromatin or the coiled body, suggesting SNAI2 is associated with active transcription or active splicing regions.
  • 组织表达: Expressed in most adult human tissues, including spleen, thymus, prostate, testis, ovary, small intestine, colon, heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Not detected in peripheral blood leukocyte. Expressed in the dermis and in all layers of the epidermis, with high levels of expression in the basal layers (at protein level). Expressed in osteoblasts (at protein level). Expressed in mesenchymal stem cells (at protein level). Expressed in breast tumor cells (at protein level).
  • 科研货号: PLA021440
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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