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TFIIH p89 Monoclonal Antibody

说明书

BYab-01057

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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产品简介>

宿主
反应性
应用
WB
分子量(DA)
免疫原
Purified recombinant human TFIIH p89 (C-terminus) protein fragments expressed in E.coli.
特异性
TFIIH p89 Monoclonal Antibody detects endogenous levels of TFIIH p89 protein.
来源
Monoclonal, Mouse
组成(Formulation)
Purified mouse monoclonal in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
稀释比例
Western Blot: 1/1000 - 1/2000. Not yet tested in other applications.
纯化工艺(Immunogen)
Affinity purification
浓度
1 mg/ml
背景(Background)
This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014],
功能
disease:Defects in ERCC3 are a cause of trichothiodystrophy photosensitive (TTDP) [MIM:601675]. TTDP is an autosomal recessive disease characterized by sulfur-deficient brittle hair and nails, ichthyosis, mental retardation, impaired sexual development, abnormal facies and cutaneous photosensitivity correlated with a nucleotide excision repair (NER) defect. Neonates with trichothiodystrophy and ichthyosis are usually born with a collodion membrane. The severity of the ichthyosis after the membrane is shed is variable, ranging from a mild to severe lamellar ichthyotic phenotype. There are no reports of skin cancer associated with TTDP.,disease:Defects in ERCC3 are the cause of xeroderma pigmentosum complementation group B (XP-B) [MIM:610651]; also known as xeroderma pigmentosum II (XP2) or XP group B (XPB) or xeroderma pigmentosum group B combined with Cockayne syndrome (XP-B/CS). Xeroder
基因名称(Gene Name)
ERCC3
蛋白名称
TFIIH basal transcription factor complex helicase XPB subunit
简称
TFIIH
其他名称
ERCC3; XPB; XPBC; TFIIH basal transcription factor complex helicase XPB subunit; Basic transcription factor 2 89 kDa subunit; BTF2 p89; DNA excision repair protein ERCC-3; DNA repair protein complementing XP-B cells; TFIIH basal transcripti
Fields
>>Basal transcription factors;>>Nucleotide excision repair
人基因ID
2071
人蛋白质序列数据库
P19447
小鼠基因ID
13872
小鼠蛋白质序列数据库
P49135
大鼠基因ID
291703
大鼠蛋白质序列数据库
Q4G005
细胞定位
Nucleus.
组织表达
Adipose tissue,Epithelium,Placenta,
储存(Storage)
-20°C/1 year

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TFIIH p89 Monoclonal Antibody

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