Septin 9 抗体 (AA 15-282)
Quick Overview for Septin 9 抗体 (AA 15-282) (ABIN7600104)
抗原
See all Septin 9 (SEPT9) 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 15-282
-
原理
- Anti-MSF/SEPTIN9 Antibody Picoband®
-
交叉反应 （详细）
- No cross-reactivity with other proteins.
-
产品特性
- Anti-MSF/SEPTIN9 Antibody Picoband® (ABIN7600104). Tested in ELISA, Flow Cytometry, IF, IHC, WB applications. This antibody reacts with Human, Mouse. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
-
纯化方法
- Immunogen affinity purified.
-
免疫原
- E.coli-derived human MSF/SEPTIN9 recombinant protein (Position: R15-D282).
-
亚型
- IgG
-
-
anti-Septin 9 (SEPT9) (AA 57-85), (C-Term) antibody
SEPT9 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB1931 unconjugated
anti-Septin 9 (SEPT9) (AA 26-125) antibodySEPT9 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠, 豚鼠, 斑马鱼, 猴, 小鸡, Hamster WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) antibodySEPT9 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 26-125) antibodySEPT9 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2C6 unconjugated
anti-Septin 9 (SEPT9) (AA 1-568) antibodySEPT9 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 1-110) antibodySEPT9 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) antibodySEPT9 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (Middle Region) antibodySEPT9 适用: 人, 小鼠, 大鼠, 豚鼠, 斑马鱼, Cow, 犬, 马, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
Western blot, 0.25-0.5 μg/mL, Human
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human, Mouse
Immunofluorescence, 5 μg/mL, Human
Flow Cytometry(Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL, -
1. Collie, A. M. B., Landsverk, M. L., Ruzzo, E., Mefford, H. C., Buysse, K., Adkins, J. R., Knutzen, D. M., Barnett, K., Brown, R. H., Jr., Parry, G. J., Yum, S. W., Simpson, D. A., Olney, R. K., Chinnery, P. F., Eichler, E. E., Chance, P. F., Hannibal, M. C. Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. J. Med. Genet. 47: 601-607, 2010. 2. Hannibal, M. C., Ruzzo, E. K., Miller, L. R., Betz, B., Buchan, J. G., Knutzen, D. M., Barnett, K., Landsverk, M. L., Brice, A., LeGuern, E., Bedford, H. M., Worrall, B. B., Lovitt, S., Appel, S. H., Andermann, E., Bird, T. D., Chance, P. F. SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. Neurology 72: 1755-1759, 2009. 3. Kalikin, L. M., Sims, H. L., Petty, E. M. Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors. Genomics 63: 165-172, 2000. -
限制
- 仅限研究用
-
-
-
状态
- Lyophilized
-
溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
-
浓度
- 500 μg/mL
-
缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
-
储存条件
- 4 °C,-20 °C
-
储存方法
-
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
-
-
- Septin 9 (SEPT9)
-
别名
- SEPTIN9
-
背景
-
Synonyms: Aldo-keto reductase family 1 member D1, 3-oxo-5-beta-steroid 4-dehydrogenase, Delta (4)-3-ketosteroid 5-beta-reductase, Delta (4)-3-oxosteroid 5-beta-reductase, AKR1D1, SRD5B1
Tissue Specificity: Highly expressed in liver. Expressed in testis and weakly in colon.
Background: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
-
分子量
- 70 kDa
-
基因ID
- 10801
抗原
-
