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SMAL1 rabbit pAb
商品货号: PLA009064
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 基因名称: SMARCAL1 HARP
  • 蛋白名称: SMAL1
  • Human_gene_id: 50485
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50485
  • Human_swiss_prot_no: Q9NZC9
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9NZC9/entry
  • Mouse_gene_id: 54380
  • Mouse_gene_link: https://www.uniprot.org/uniprot/54380
  • Mouse_swiss_prot_no: Q8BJL0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8BJL0
  • Rat_gene_id: 316477
  • Rat_gene_link: https://www.uniprot.org/uniprot/316477
  • Rat_swiss_prot_no: B4F769
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/B4F769
  • 特异性: This antibody detects endogenous levels of SMAL1 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
  • 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: SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1 (EC 3.6.4.-) (HepA-related protein) (hHARP) (Sucrose nonfermenting protein 2-like 1)
  • 实测条带: 105kD
  • 功能: disease:Defects in SMARCAL1 are a cause of Schimke immuno-osseous dysplasia (SIOD) [MIM:242900]. SIOD causes spondyloepiphyseal dysplasia, renal dysfunction and T-cell immunodeficiency. Approximately half of all patients also exhibit hyperthyroidism, while around half also exhibit episodal cerebral ischema.,function:ATP-dependent annealing helicase that catalyzes the rewinding of the stably unwound DNA. Rewinds single-stranded DNA bubbles that are stably bound by replication protein A (RPA). Acts throughout the genome to reanneal stably unwound DNA, performing the opposite reaction of many enzymes, such as helicases and polymerases, that unwind DNA.,online information:SMARCAL1 mutation db,similarity:Belongs to the SNF2/RAD54 helicase family. SMARCAL1 subfamily.,similarity:Contains 1 helicase ATP-binding domain.,similarity:Contains 1 helicase C-terminal domain.,similarity:Contains 2 HARP domains.,tissue specificity:Ubiquitously expressed, with high levels in testis.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Recruited to damaged DNA regions.
  • 组织表达: Ubiquitously expressed, with high levels in testis.
  • 科研货号: PLA009064
SMAL1 rabbit pAb
Catalog No PLA009064
Product information
  • 基因名称: SMARCAL1 HARP
  • 蛋白名称: SMAL1
  • Human_gene_id: 50485
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50485
  • Human_swiss_prot_no: Q9NZC9
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9NZC9/entry
  • Mouse_gene_id: 54380
  • Mouse_gene_link: https://www.uniprot.org/uniprot/54380
  • Mouse_swiss_prot_no: Q8BJL0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8BJL0
  • Rat_gene_id: 316477
  • Rat_gene_link: https://www.uniprot.org/uniprot/316477
  • Rat_swiss_prot_no: B4F769
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/B4F769
  • 特异性: This antibody detects endogenous levels of SMAL1 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
  • 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: SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1 (EC 3.6.4.-) (HepA-related protein) (hHARP) (Sucrose nonfermenting protein 2-like 1)
  • 实测条带: 105kD
  • 功能: disease:Defects in SMARCAL1 are a cause of Schimke immuno-osseous dysplasia (SIOD) [MIM:242900]. SIOD causes spondyloepiphyseal dysplasia, renal dysfunction and T-cell immunodeficiency. Approximately half of all patients also exhibit hyperthyroidism, while around half also exhibit episodal cerebral ischema.,function:ATP-dependent annealing helicase that catalyzes the rewinding of the stably unwound DNA. Rewinds single-stranded DNA bubbles that are stably bound by replication protein A (RPA). Acts throughout the genome to reanneal stably unwound DNA, performing the opposite reaction of many enzymes, such as helicases and polymerases, that unwind DNA.,online information:SMARCAL1 mutation db,similarity:Belongs to the SNF2/RAD54 helicase family. SMARCAL1 subfamily.,similarity:Contains 1 helicase ATP-binding domain.,similarity:Contains 1 helicase C-terminal domain.,similarity:Contains 2 HARP domains.,tissue specificity:Ubiquitously expressed, with high levels in testis.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Recruited to damaged DNA regions.
  • 组织表达: Ubiquitously expressed, with high levels in testis.
  • 科研货号: PLA009064
  • 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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