Anti-FOXL2抗体(ab5096)
Key features and details
- Goat polyclonal to FOXL2
- Suitable for: WB
- Reacts with: Human
- Isotype: IgG
选择批间可重复性更高的重组抗体
- 研究可靠 —— 各批次间结果一致且可重复
- 长期批量供应 —— 采用重组技术，可实现快速生产
- 首次实验即可成功 —— 经过大量验证确认了特异性
- 符合伦理标准 —— 产品不含动物成分
概述
-
产品名称
Anti-FOXL2抗体
参阅全部 FOXL2 一抗 -
描述
山羊多克隆抗体to FOXL2 -
宿主
Goat -
经测试应用
适用于: WBmore details -
种属反应性
与反应: Human
预测可用于: Mouse, Rat, Cow
-
免疫原
Synthetic peptide corresponding to FOXL2 aa 364-376 (C terminal).
Sequence:DSKTGALHSRLDL
-
阳性对照
- WB: K562 and HeLa cell lysates.
-
常规说明
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
性能
-
形式
Liquid -
存放说明
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles. -
存储溶液
pH: 7.30
Preservative: 0.02% Sodium azide
Constituents: Tris buffered saline, 0.5% BSA -
Concentration information loading... -
纯度
Immunogen affinity purified -
纯化说明
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide. -
克隆
多克隆 -
同种型
IgG -
研究领域
相关产品
-
Compatible Secondaries
-
Isotype control
应用
| 应用 | Ab评论 | 说明 |
|---|---|---|
| WB | (2) |
Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 45-50 kDa (predicted molecular weight: 43 kDa).
Primary incubation 1 hour at room temperature. |
| 说明 |
|---|
|
WB
Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 45-50 kDa (predicted molecular weight: 43 kDa). Primary incubation 1 hour at room temperature. |
靶标
-
功能
Transcriptional regulator. Critical factor essential for ovary differentiation and maintenance, and repression of the genetic program for somatic testis determination. Prevents trans-differentiation of ovary to testis throught transcriptional repression of the Sertoli cell-promoting gene SOX9 (By similarity). Has apoptotic activity in ovarian cells. Suppresses ESR1-mediated transcription of PTGS2/COX2 stimulated by tamoxifen (By similarity). Is a regulator of CYP19 expression (By similarity). Participates in SMAD3-dependent transcription of FST via the intronic SMAD-binding element (By similarity). Is a transcriptional repressor of STAR. Activates SIRT1 transcription under cellular stress conditions. Activates transcription of OSR2. -
组织特异性
In addition to its expression in the developing eyelid, it is transcribed very early in somatic cells of the developing gonad (before sex determination) and its expression persists in the follicular cells of the adult ovary. -
疾病相关
Defects in FOXL2 are a cause of blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) [MIM:110100]; also known as blepharophimosis syndrome. It is an autosomal dominant disorder characterized by eyelid dysplasia, small palpebral fissures, drooping eyelids and a skin fold running inward and upward from the lower lid. In type I BPSE (BPES1) eyelid abnormalities are associated with female infertility. Affected females show an ovarian deficit due to primary amenorrhea or to premature ovarian failure (POF). In type II BPSE (BPES2) affected individuals show only the eyelid defects. There is a mutational hotspot in the region coding for the poly-Ala domain, since 30% of all mutations in the ORF lead to poly-Ala expansions, resulting mainly in BPES type II.
Defects in FOXL2 are a cause of premature ovarian failure type 3 (POF3) [MIM:608996]. An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. -
序列相似性
Contains 1 fork-head DNA-binding domain. -
翻译后修饰
Sumoylated by SUMO1; sumoylation is required for transcriptional repression activity. -
细胞定位
Nucleus. - Information by UniProt
-
数据库链接
- Entrez Gene: 281770 Cow
- Entrez Gene: 668 Human
- Entrez Gene: 26927 Mouse
- Entrez Gene: 367152 Rat
- Omim: 605597 Human
- SwissProt: Q6VFT7 Cow
- SwissProt: P58012 Human
- SwissProt: O88470 Mouse
see all -
别名
- Blepharophimosis antibody
- Blepharophimosis epicanthus inversus and ptosis 1 antibody
- Blepharophimosis epicanthus inversus and ptosis antibody
see all
图片
-
Western blot - Anti-FOXL2 antibody (ab5096)All lanes : Anti-FOXL2 antibody (ab5096) at 2 µg/ml
Lane 1 : K562 cell lysate, 35µg protein in RIPA buffer
Lanes 2 & 4 : K562 cell lysate incubated with immunizing peptide, 35µg protein in RIPA buffer
Lane 3 : HeLa cell lysate, 35µg protein in RIPA buffer
Developed using the ECL technique.
Predicted band size: 43 kDa
Observed band size: 35 kDa why is the actual band size different from the predicted?Primary incubation 1 hour at room temperature.
实验方案
数据表及文件
-
SDS download
-
Datasheet download
文献 (57)
ab5096 被引用在 57 文献中.
- Ford EA et al. Transcriptomic profiling of neonatal mouse granulosa cells reveals new insights into primordial follicle activation†. Biol Reprod 106:503-514 (2022). PubMed: 34673933
- Oikawa M et al. Generation of Tfap2c-T2A-tdTomato knock-in reporter rats via adeno-associated virus-mediated efficient gene targeting. Mol Reprod Dev 89:129-132 (2022). PubMed: 35170139
- Agrimson KS et al. Lrh1 can help reprogram sexual cell fate and is required for Sertoli cell development and spermatogenesis in the mouse testis. PLoS Genet 18:e1010088 (2022). PubMed: 35192609
- Alhasnani MA et al. Interaction between mono-(2-ethylhexyl) phthalate and retinoic acid alters Sertoli cell development during fetal mouse testis cord morphogenesis. Curr Res Toxicol 3:100087 (2022). PubMed: 36189433
- Fan X et al. Single-Cell Transcriptomics Analysis of Human Small Antral Follicles. Int J Mol Sci 22:N/A (2021). PubMed: 34769386