POMT2 抗体 (AA 500-560)
Quick Overview for POMT2 抗体 (AA 500-560) (ABIN2747315)
抗原
See all POMT2 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 500-560
-
交叉反应
- 小鼠
-
交叉反应 （详细）
- The antibody does not cross react to any other cellular protein.
-
产品特性
- POMT2- selective antibodies were generated against a peptide taken from the N-terminal region of the human protein. The POMT2-selective antibodies are affinity purified on an immobilized antigen based affinity matrix, the isolated antibodies were then stabilized in antibody stabilization buffer for long-term storage. The anti- POMT2-selective antibodies are fully characterized for applications in western blotting and ELISA at the recommended dilutions. antibodies-online.com provides POMT2 Western blot positive control samples in SDS-PAGE sample buffer.
-
纯化方法
- Affinity Purified
-
免疫原
- Synthetic peptide taken within amino acid region 500-560 on human POMT2 protein.
-
亚型
- IgG
-
-
anti-Protein-O-Mannosyltransferase 2 (POMT2) (AA 483-580) antibody
POMT2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1D9 unconjugated
anti-Protein-O-Mannosyltransferase 2 (POMT2) (AA 483-580) antibodyPOMT2 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Protein-O-Mannosyltransferase 2 (POMT2) (AA 434-483) antibodyPOMT2 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, 兔, 斑马鱼, 猴, Bat, 小鸡, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Protein-O-Mannosyltransferase 2 (POMT2) (Middle Region) antibodyPOMT2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
Antibodies were tested in ELISA and western blotting applications at 1:500 dilution using ABIN1686546 samples. Antibody dilutions for these antibodies are for reference only, investigators are expected to determine the optimal conditions.Application of this antibody in other protocols has not yet tested.
WB: > 1:500
IMM & IP pull-down assays: n.d.
IHC: n.d.
Investigators using this antibody in protocols other than listed above can request a complimentary sample of this antibody. n.d. not necessarily means the antibody is not suitable for that application, it simply means we have not yet characterized the antibody for that application.
The antibody labels a strong band of POMT2 at 90 kDa in ABIN1686546 samples and in other cancer cell lines. -
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 0.55-0.75 μg/μL
-
储存条件
- -20 °C
-
储存方法
- Storage of very dilute antibody solutions is not recommended.
-
-
- POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))
-
别名
- POMT2
-
背景
- Protein O mannosylation is initiated in the endoplasmic reticulum by protein O-mannosyl transferases (POMT proteins). They play an important role in the secretion, localization, and function of many proteins, as well as in cell wall integrity and morphogenesis in fungi. On the molecular level, the O-mannosylation pathway and the function of O-mannosyl glycans are characterized best in the eukaryotic model yeast Saccharomyces cerevisiae. O-mannosylation defects interfere with cell wall integrity and ER homeostasis in yeast, resulting in severe neuromuscular diseases in humans. Transfer of this knowledge from yeast to mammals could lead to the development of novel antifungal drugs by diagnostic and therapeutic approaches in the frame of neuromuscular diseases. The POMT family is classified into POMT1, POMT2 and POMT4 subfamilies. Protein-O-Mannosyl Transferase 2 (POMT2) encodes an integral membrane protein which localizes to the endoplasmic reticulum. It shares significant sequence similarity with the family of protein O-mannosyl transferases of S. cerevisiae. This 750 amino acid protein has a seven transmembrane helical structure with a central hydrophilic domain surrounded by five N-terminal and two C-terminal transmembrane regions. Like other known members of its family, POMT2 lacks a characteristic ER-targeting or -retention signal and contains five N-glycosylation sites. POMT2 shares 36 % sequence identity with human POMT1 and RNA dot blot analysis reveals highest expression of mouse POMT2 in testis. POMT2 mutations have been identified in congenital muscular dystrophy (CMD) cases with a wide range of of clinical involvement, ranging from the severe muscle-eye-brain disease and Walker-Warburg syndrome to limb girdle muscular dystrophy without structural brain or ocular involvement. The gene for POMT2 is present on chromosome 14q24.3
-
UniProt
- Q9UKY4
抗原
-
