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Bethyl Laboratories
TEIF Polyclonal Antibody
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TEIF Antibody (A302-653A) in WB
Detection of human and mouse TEIF by western blot (h&m) and immunoprecipitation (h). Samples: Whole cell lysate from HeLa (5, 15 and 50 µg for WB; 1 mg for IP, 20% of IP loaded), HEK293T (T; 50 µg), and mouse NIH 3T3 (M; 50 µg) cells. Antibodies: Affinity purified rabbit anti-TEIF antibody (Product # A302-653A) used for WB at 0.04 µg/mL (A) and 1 µg/mL (B) and used for IP at 3 µg/mg lysate. TEIF was also immunoprecipitated by rabbit anti-TEIF antibody A302-652A, which recognizes an upstream epitope. Detection: Chemiluminescence with exposu... View More
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
产品信息
A302-653A
产品规格
种属反应
Human,
Mouse
宿主/亚型
Rabbit
/ IgG
分类
Polyclonal
类型
Antibody
抗原
Region between residue 758 and 808 of Human telomerase transcriptional elements-interacting factor.
偶联物
Unconjugated
Unconjugated
Unconjugated
形式
Liquid
浓度
0.20 mg/mL
规格
20 µg
纯化类型
Antigen affinity chromatography
保存液
TBS, pH 7.0 to 8.0, with 0.1% BSA
内含物
0.09% sodium azide
保存条件
4°C
运输条件
Ambient (domestic); Wet ice (international)
产品详细信息
The recommended shelf life for this product is 1 year from date of receipt.
靶标信息
With approximately 135 million base pairs and 1,400 genes, chromosome 11 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 β 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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
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生物信息学
蛋白别名: 105 kDa kinase-like protein; coated vesicle-associated kinase of 90 kDa; likely ortholog of mouse N-terminal kinase-like protein; mitosis-associated kinase-like protein NTKL; SCY1-like protein 1; SCY1-like, kinase-like 1; telomerase regulation-associated protein; telomerase transcriptional elements-interacting factor; teratoma-associated tyrosine kinase; TRAP; ubiquitous protein kinase-like (105 kDa); unnamed protein product
基因别名: 2810011O19Rik; GKLP; HT019; mdf; mfd; NKTL; NTKL; P105; SCAR21; TAPK; TEIF; TRAP
UniProt ID: (Human) Q96KG9, (Mouse) Q9EQC5
Entrez Gene ID: (Human) 57410, (Mouse) 78891
Disclaimer
Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.
