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CTDP1 rabbit pAb
商品货号: PLA009089
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: CTDP1 FCP1
  • 蛋白名称: CTDP1
  • Human_gene_id: 9150
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=9150
  • Human_swiss_prot_no: Q9Y5B0
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y5B0/entry
  • Mouse_gene_id: 67655
  • Mouse_gene_link: https://www.uniprot.org/uniprot/67655
  • Mouse_swiss_prot_no: Q7TSG2
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q7TSG2
  • 特异性: This antibody detects endogenous levels of CTDP1 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: RNA polymerase II subunit A C-terminal domain phosphatase (EC 3.1.3.16) (TFIIF-associating CTD phosphatase)
  • 实测条带: 105kD
  • 功能: catalytic activity:A phosphoprotein + H(2)O = a protein + phosphate.,disease:Defects in CTDP1 are a cause of congenital cataracts facial dysmorphism and neuropathy syndrome (CCFDN) [MIM:604168]. CCFDN is an autosomal recessive developmental disorder that occurs in an endogamous group of Vlax Roma (Gypsies). The syndrome is characterized by a complex clinical phenotype with seemingly unrelated features involving multiple organs and systems. Developmental abnormalities include congenital cataracts and microcorneae, hypomyelination of the peripheral nervous system, impaired physical growth, delayed early motor and intellectual development, facial dysmorphism and hypogonadism. Central nervous system involvement, with cerebral and spinal cord atrophy, may be the result of disrupted development with superimposed degenerative changes. Affected individuals are prone to severe rhabdomyolysis after viral infections and to serious complications related to general anesthesia (such as pulmonary edema and epileptic seizures).,function:Processively dephosphorylates 'Ser-2' and 'Ser-5' of the heptad repeats YSPTSPS in the C-terminal domain of the largest RNA polymerase II subunit. This promotes the activity of RNA polymerase II.,PTM:Phosphorylated. In the presence of TFIIF, the phosphorylated form has an increased CTD phosphatase activity. The phosphorylation is required for the physical interaction with GTF2F1.,similarity:Contains 1 BRCT domain.,similarity:Contains 1 FCP1 homology domain.,subunit:Homodimer. Interacts with GTF2F1. Interacts with WDR77, SNRPB and SNRNP70.,tissue specificity:Ubiquitously expressed. Isoform 3 is expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and placenta.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton, spindle pole . Midbody . Found at centrosomes in prometaphase, at spindle and spindle poles in metaphase and at spindle midzone and midbody in anaphase and telophase-G1 respectively.
  • 组织表达: Ubiquitously expressed.
  • 科研货号: PLA009089
CTDP1 rabbit pAb
Catalog No PLA009089
Product information
  • 基因名称: CTDP1 FCP1
  • 蛋白名称: CTDP1
  • Human_gene_id: 9150
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=9150
  • Human_swiss_prot_no: Q9Y5B0
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y5B0/entry
  • Mouse_gene_id: 67655
  • Mouse_gene_link: https://www.uniprot.org/uniprot/67655
  • Mouse_swiss_prot_no: Q7TSG2
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q7TSG2
  • 特异性: This antibody detects endogenous levels of CTDP1 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: RNA polymerase II subunit A C-terminal domain phosphatase (EC 3.1.3.16) (TFIIF-associating CTD phosphatase)
  • 实测条带: 105kD
  • 功能: catalytic activity:A phosphoprotein + H(2)O = a protein + phosphate.,disease:Defects in CTDP1 are a cause of congenital cataracts facial dysmorphism and neuropathy syndrome (CCFDN) [MIM:604168]. CCFDN is an autosomal recessive developmental disorder that occurs in an endogamous group of Vlax Roma (Gypsies). The syndrome is characterized by a complex clinical phenotype with seemingly unrelated features involving multiple organs and systems. Developmental abnormalities include congenital cataracts and microcorneae, hypomyelination of the peripheral nervous system, impaired physical growth, delayed early motor and intellectual development, facial dysmorphism and hypogonadism. Central nervous system involvement, with cerebral and spinal cord atrophy, may be the result of disrupted development with superimposed degenerative changes. Affected individuals are prone to severe rhabdomyolysis after viral infections and to serious complications related to general anesthesia (such as pulmonary edema and epileptic seizures).,function:Processively dephosphorylates 'Ser-2' and 'Ser-5' of the heptad repeats YSPTSPS in the C-terminal domain of the largest RNA polymerase II subunit. This promotes the activity of RNA polymerase II.,PTM:Phosphorylated. In the presence of TFIIF, the phosphorylated form has an increased CTD phosphatase activity. The phosphorylation is required for the physical interaction with GTF2F1.,similarity:Contains 1 BRCT domain.,similarity:Contains 1 FCP1 homology domain.,subunit:Homodimer. Interacts with GTF2F1. Interacts with WDR77, SNRPB and SNRNP70.,tissue specificity:Ubiquitously expressed. Isoform 3 is expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and placenta.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton, spindle pole . Midbody . Found at centrosomes in prometaphase, at spindle and spindle poles in metaphase and at spindle midzone and midbody in anaphase and telophase-G1 respectively.
  • 组织表达: Ubiquitously expressed.
  • 科研货号: PLA009089
  • 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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