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MAMD1 rabbit pAb
商品货号: PLA009190
适 应 性: 人,小鼠
WB
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: MAMLD1 CG1 CXorf6
  • 蛋白名称: MAMD1
  • Human_gene_id: 10046
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=10046
  • Human_swiss_prot_no: Q13495
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q13495/entry
  • Mouse_gene_id: 333639
  • Mouse_gene_link: https://www.uniprot.org/uniprot/333639
  • Mouse_swiss_prot_no: P0C6A2
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P0C6A2
  • 特异性: This antibody detects endogenous levels of MAMD1 at Human/Mouse
  • 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
  • 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: Mastermind-like domain-containing protein 1 (F18) (Protein CG1)
  • 实测条带: 85kD
  • 功能: caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in MAMLD1 are a cause of X-linked hypospadias type 2 (HYSP2) [MIM:300758]. Hypospadias is a common malformation in which the urethra opens on the ventral side of the penis. It is considered a complex disorder with both genetic and environmental factors involved in the pathogenesis. Hypospadias can occur alone on an apparently multifactorial basis or as part of syndromes.,similarity:Belongs to the mastermind family.,tissue specificity:Preferentially expressed in skeletal muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Punctate nuclear localization.
  • 组织表达: Expressed in fetal brain, fetal ovary and fetal testis. Expressed in adult brain, ovary, skin, testis, uterus. Highly expressed in skeletal muscle.
  • 科研货号: PLA009190
MAMD1 rabbit pAb
Catalog No PLA009190
Product information
  • 基因名称: MAMLD1 CG1 CXorf6
  • 蛋白名称: MAMD1
  • Human_gene_id: 10046
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=10046
  • Human_swiss_prot_no: Q13495
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q13495/entry
  • Mouse_gene_id: 333639
  • Mouse_gene_link: https://www.uniprot.org/uniprot/333639
  • Mouse_swiss_prot_no: P0C6A2
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P0C6A2
  • 特异性: This antibody detects endogenous levels of MAMD1 at Human/Mouse
  • 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
  • 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: Mastermind-like domain-containing protein 1 (F18) (Protein CG1)
  • 实测条带: 85kD
  • 功能: caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in MAMLD1 are a cause of X-linked hypospadias type 2 (HYSP2) [MIM:300758]. Hypospadias is a common malformation in which the urethra opens on the ventral side of the penis. It is considered a complex disorder with both genetic and environmental factors involved in the pathogenesis. Hypospadias can occur alone on an apparently multifactorial basis or as part of syndromes.,similarity:Belongs to the mastermind family.,tissue specificity:Preferentially expressed in skeletal muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Punctate nuclear localization.
  • 组织表达: Expressed in fetal brain, fetal ovary and fetal testis. Expressed in adult brain, ovary, skin, testis, uterus. Highly expressed in skeletal muscle.
  • 科研货号: PLA009190
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
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