TCRP1,舌癌化疗耐药相关蛋白1抗体-抗体-抗体-生物在线
上海沪震实业有限公司
TCRP1,舌癌化疗耐药相关蛋白1抗体

TCRP1,舌癌化疗耐药相关蛋白1抗体

商家询价

产品名称: TCRP1,舌癌化疗耐药相关蛋白1抗体

英文名称: Anti-TCRP1 antibody

产品编号: HZ-8199R

产品价格: null

产品产地: 中国/美国

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: WB,ELISA,IHC-P,IHC-F,IF

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TCRP1,舌癌化疗耐药相关蛋白1抗体

产品编号HZ-8199R
英文名称TCRP1
中文名称舌癌化疗耐药相关蛋白1
别 名F168A_HUMAN; Fam168a; KIAA0280; Protein FAM168A; TCRP1; Tongue cancer chemotherapy resistance-associated protein 1.
说 明 书0.1ml 0.2ml
研究领域肿瘤 细胞生物
抗体来源Rabbit
克隆类型Polyclonal
交叉反应 Human, Mouse, Rat, Pig, Cow, Sheep,
TCRP1,舌癌化疗耐药相关蛋白1抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量26kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human FAM168A/TCRP1
亚 型IgG
纯化方法affinity purified by Protein A
储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
TCRP1,舌癌化疗耐药相关蛋白1抗体PubMedPubMed
产品介绍background:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

Subunit:
May interact with FAM168B.

Similarity:
Belongs to the FAM168 protein family.

TCRP1,舌癌化疗耐药相关蛋白1抗体Database links:
UniProtKB/Swiss-Prot: Q92567.2

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.