TCEANC2 抗体 (HRP)
Quick Overview for TCEANC2 抗体 (HRP) (ABIN1422550)
抗原
See all TCEANC2 抗体适用
宿主
克隆类型
标记
应用范围
-
-
交叉反应
- 人, 小鼠, 大鼠
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human C1orf83
-
亚型
- IgG
-
-
anti-Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2) (AA 1-208) antibody
TCEANC2 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2) (AA 1-208), (N-Term) antibodyTCEANC2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2) (N-Term) antibodyTCEANC2 适用: 人, 大鼠, 小鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2) (N-Term) antibodyTCEANC2 适用: 人, 大鼠, 小鼠, Cow WB 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
WB 1:300-5000
IHC-P 1:200-400 -
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1 μg/μL
-
缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
-
储存液
- ProClin
-
注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
-
注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
-
储存条件
- -20 °C
-
储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
-
有效期
- 12 months
-
-
- TCEANC2 (Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2))
-
别名
- C1orf83
-
背景
-
Synonyms: chromosome 1 open reading frame 83, FLJ32112, FLJ39169, hypothetical protein LOC127428, Uncharacterized protein C1orf83, TEAN2_HUMAN.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf83 gene product has been provisionally designated C1orf83 pending further characterization. There are two isoforms of C1orf83 that are produced as a result of alternative splicing events.
-
基因ID
- 127428
抗原
-
