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ASPM Polyclonal Antibody
商品货号: PLA007511
适 应 性: 人,大鼠,小鼠,
IHC IF
¥600元
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MSDS
说明书
商品描述
  • 基因名称: ASPM MCPH5
  • 蛋白名称: Abnormal spindle-like microcephaly-associated protein (Abnormal spindle protein homolog) (Asp homolog)
  • Human_gene_id: 259266
  • Human_swiss_prot_no: Q8IZT6
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q8IZT6/entry
  • Mouse_swiss_prot_no: Q8CJ27
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8CJ27
  • 特异性: ASPM Polyclonal Antibody detects endogenous levels of protein.
  • 组成: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: IHC-p 1:50-300. 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
  • 实测条带: 382kD
  • 功能: disease:Defects in ASPM are the cause of microcephaly primary type 5 (MCPH5) [MIM:608716]; also known as true microcephaly or microcephaly vera. Microcephaly is defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits. This entity is inherited as autosomal recessive trait.,function:Probable role in mitotic spindle regulation and coordination of mitotic processes (By similarity). May have a preferential role in regulating neurogenesis.,similarity:Contains 2 CH (calponin-homology) domains.,similarity:Contains 39 IQ domains.,subcellular location:The nuclear-cytoplasmic distribution could be regulated by the availability of calmodulin.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm . Cytoplasm, cytoskeleton, spindle . Nucleus . The nuclear-cytoplasmic distribution could be regulated by the availability of calmodulin (By similarity). Localizes to spindle poles during mitosis (PubMed:19690332). Associates with microtubule minus ends (By similarity). .
  • 组织表达: Colon adenocarcinoma,Epithelium,Fetal brain,Kidney,Lymph,Tongue,
  • 科研货号: PLA007511
ASPM Polyclonal Antibody
Catalog No PLA007511
Product information
  • 基因名称: ASPM MCPH5
  • 蛋白名称: Abnormal spindle-like microcephaly-associated protein (Abnormal spindle protein homolog) (Asp homolog)
  • Human_gene_id: 259266
  • Human_swiss_prot_no: Q8IZT6
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q8IZT6/entry
  • Mouse_swiss_prot_no: Q8CJ27
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8CJ27
  • 特异性: ASPM Polyclonal Antibody detects endogenous levels of protein.
  • 组成: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: IHC-p 1:50-300. 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
  • 实测条带: 382kD
  • 功能: disease:Defects in ASPM are the cause of microcephaly primary type 5 (MCPH5) [MIM:608716]; also known as true microcephaly or microcephaly vera. Microcephaly is defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits. This entity is inherited as autosomal recessive trait.,function:Probable role in mitotic spindle regulation and coordination of mitotic processes (By similarity). May have a preferential role in regulating neurogenesis.,similarity:Contains 2 CH (calponin-homology) domains.,similarity:Contains 39 IQ domains.,subcellular location:The nuclear-cytoplasmic distribution could be regulated by the availability of calmodulin.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm . Cytoplasm, cytoskeleton, spindle . Nucleus . The nuclear-cytoplasmic distribution could be regulated by the availability of calmodulin (By similarity). Localizes to spindle poles during mitosis (PubMed:19690332). Associates with microtubule minus ends (By similarity). .
  • 组织表达: Colon adenocarcinoma,Epithelium,Fetal brain,Kidney,Lymph,Tongue,
  • 科研货号: PLA007511
  • 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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