重组Anti-JAK2 (phospho Y1007 + Y1008)抗体[E132] (ab32101)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [E132] to JAK1 (phospho Y1034 + Y1035) + JAK2 (phospho Y1007 + Y1008)
- Suitable for: ELISA, Flow Cyt (Intra), WB, ICC/IF, IHC-P, Dot blot
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
概述
-
产品名称
Anti-JAK2 (phospho Y1007 + Y1008)抗体[E132] -
描述
兔单克隆抗体[E132] to JAK1 (phospho Y1034 + Y1035) + JAK2 (phospho Y1007 + Y1008) -
宿主
Rabbit -
特异性
This antibody is phospho-specific and only detects phosphorylated JAK2 on Tyrosine 1007 and 1008 (pY1007+Y1008) and JAK1 on Tyrosine 1034 and 1035 (pY1034+Y1035). According to our ELISA results, this antibody preferentially recognizes phospho Y1007. Stimulation may be required to allow detection of the phosphorylated protein. Please see images below for recommended treatment conditions and positive controls.
The mouse and rat recommendation is based on the WB results. We do not guarantee IHC-P for mouse and rat.
-
经测试应用
适用于: ELISA, Flow Cyt (Intra), WB, ICC/IF, IHC-P, Dot blotmore details -
种属反应性
与反应: Mouse, Rat, Human -
免疫原
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
-
阳性对照
- WB: Hepa1-6, MEF, C6, Jurkat treated with Pervanadate and Jurkat cell lysates. IHC-P: Human differentiated squamous cell carcinoma tissue. ICC/IF: Jurkat cells (treated with Pervanadate). Flow Cyt (intra): Jurkat starved of serum for 16 hours then treated with 1mM Pervanadate for 30 minutes.
-
常规说明
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
性能
-
形式
Liquid -
存放说明
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle. -
存储溶液
pH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 49% PBS, 50% Glycerol (glycerin, glycerine), 0.05% BSA -
Concentration information loading...
-
纯度
Protein A purified -
克隆
单克隆 -
克隆编号
E132 -
同种型
IgG -
研究领域
相关产品
-
Alternative Versions
- Alexa Fluor® 488 Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab200339)
- Alexa Fluor® 647 Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab200340)
- Alexa Fluor® 594 Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab201744)
- Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] - BSA and Azide free (ab219728)
- Alexa Fluor® 568 Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab312579)
- Alexa Fluor® 750 Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab321572)
-
Compatible Secondaries
-
Isotype control
-
Recombinant Protein
-
Related Products
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab32101于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
ELISA |
Use at an assay dependent concentration.
|
|
Flow Cyt (Intra) |
1/20.
|
|
WB | (3) |
1/1000 - 1/10000. Detects a band of approximately 120 kDa (predicted molecular weight: 130 kDa).
The samples may require stimulation (E.g., Jurkat cells treated with pervanadate for 5 min) |
ICC/IF | (1) |
1/1000.
|
IHC-P |
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
The mouse and rat recommendation is based on the WB results. We do not guarantee IHC-P for mouse and rat. |
|
Dot blot |
1/1000.
|
说明 |
---|
ELISA
Use at an assay dependent concentration. |
Flow Cyt (Intra)
1/20. |
WB
1/1000 - 1/10000. Detects a band of approximately 120 kDa (predicted molecular weight: 130 kDa). The samples may require stimulation (E.g., Jurkat cells treated with pervanadate for 5 min) |
ICC/IF
1/1000. |
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. The mouse and rat recommendation is based on the WB results. We do not guarantee IHC-P for mouse and rat. |
Dot blot
1/1000. |
靶标
-
细胞定位
JAK1: Endomembrane system. Wholly intracellular, possibly membrane associated. JAK2: Endomembrane system. Nucleus. -
数据库链接
- Entrez Gene: 3716 Human
- Entrez Gene: 3717 Human
- Entrez Gene: 16451 Mouse
- Entrez Gene: 16452 Mouse
- Entrez Gene: 24514 Rat
- Entrez Gene: 84598 Rat
- Omim: 147795 Human
- Omim: 147796 Human
see all
图片
-
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101)
ab32101 showing positive staining in Human differentiated squamous cell carcinoma of the cervix tissue at 1/10000 dilution. Goat Anti-Rabbit IgG H&L (HRP) was used as secondary antibody. Antigen retreival was carried out by Heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0).
Nuclear staining on human differentiated squamous cell carcinoma of the cervix without alkaline phosphatase treatment (image A). No staining on human differentiated squamous cell carcinoma of the cervix with alkaline phosphatase treatment (image B)
-
All lanes : Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101) at 1/1000 dilution
Lane 1 : Hepa1-6 (Mouse hepatoma epithelial cell) whole cell lysate
Lane 2 : Hepa1-6 (Mouse hepatoma epithelial cell) treated with 100 µM pervanadate for 30 minutes whole cell lysate
Lane 3 : MEF (Mouse embryonic fibroblast (immortalized)) whole cell lysate
Lane 4 : MEF (Mouse embryonic fibroblast (immortalized)) treated with 100 µM pervanadate for 30 minutes whole cell lysate
Lysates/proteins at 15 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 130 kDaThe extra bands are undefined.
-
All lanes : Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101)
Lane 1 : Mouse hippocampus lysate
Lane 2 : Mouse P240 hippocampus lysate
Lane 3 : Mouse P7 hippocampus lysate
Lane 4 : Rat hippocampus lysate
Lane 5 : Rat P7 hippocampus lysate
Lane 6 : Rat brain cortex lysate
Lane 7 : Human brain lysate
Lane 8 : Mouse brain lysate
Lane 9 : Rat brain lysate
Lane 10 : C6 (Rat glial tumor glial cell) whole cell lysate
Lane 11 : C6 (Rat glial tumor glial cell) treated with 50mM pervanadate for 5 minutes whole cell lysate
Lysates/proteins at 15 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 130 kDa -
All lanes : Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101) at 1/5000 dilution
Lane 1 : Untreated Jurkat cells whole cell lysates
Lane 2 : Jurkat cells were treated with 50mM Pervanadate for 5 minutes whole cell lysates
Lane 3 : Jurkat cells were treated with 50mM Pervanadate for 5 minutes whole cell lysates. Then the membrane was incubated with Alkaline phosphatase.
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 130 kDa
Observed band size: 120 kDa why is the actual band size different from the predicted?
Exposure time: 5 secondsBlocking and diluting buffer 5% NFDM/TBST
-
Immunocytochemistry/ Immunofluorescence - Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101)
Immunocytochemistry/Immunofluorescence analysis of Jurkat +/- pervanadate (1mM, 30min) and Jurkat + pervanadate (1mM, 30min) + LP cells labelling JAK2 (phospho Y1007 + Y1008) with ab32101 at a dilution of 1/1000. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% tritonX-100. ab150077 (goat anti-rabbit IgG Alexa Fluor® 488) (1/1000) was used as the secondary antibody. The cells were co-stained with ab195889 (Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594)) at a 1/200 dilution. Nuclei counterstained with DAPI (blue).
-
Dot blot analysis of human JAK2 (phospho Y1007 & Y1008) phospho peptide (Lane 1), JAK2 (phospho Y1007) phospho peptide (Lane 2), JAK2 (phospho Y1008) phospho peptide (Lane 3) and JAK2 non-phospho peptide (Lane 4) labelling JAK2 (phospho Y1007 & Y1008) with ab32101 at a dilution of 1/1000.
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) was used as the secondary antibody at a dilution of 1/20,000.
Blocking/Dilution buffer: 5% NFDM/TBST.
-
All lanes : Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101) at 1/1000 dilution
Lane 1 : Jurkat (Human T cell leukemia T lymphocyte) whole cell lysates
Lane 2 : Jurkat (Human T cell leukemia T lymphocyte) treated with 50mM Pervanadate for 5 minutes whole cell lysates
Lysates/proteins at 15 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 130 kDa
Observed band size: 120 kDa why is the actual band size different from the predicted?
Additional bands at: 60 kDa. We are unsure as to the identity of these extra bands.Blocking and diluting buffer: 5% NFDM/TBST
Exposure time:
Left image: 1 second
Right image: 5 minutes -
Intracellular Flow Cytometry analysis of Jurkat (human acute T cell leukemia) cells starved of serum for 16 hours then treated with 1 mM Pervanadate for 30 minutes labeling JAK2 (phospho Y1007 + Y1008) with ab32101 at 1/20 dilution (10 ug/mL) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. A Goat anti rabbit IgG (Alexa Fluorr®488) at 1/2000 dilution was used as the secondary antibody. Rabbit monoclonal IgG (Black) was used as the isotype control, cells without incubation with primary antibody and secondary antibody (Blue) was used as the unlabeled control. Unstimulated Jurkat cells were used as a negative control (Green).
-
Direct ELISA antigen dose-response curve using ab32101 at 0~1000 ng/mL. Antigen concentration of 100 ng/mL. An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) (1/2500) was used as the secondary antibody.
This antibody preferentially recognizes phospho Y1007. When the concentration of peptides is higher than 100 ng/mL, it also recognizes phospho Y1008.
-
Direct ELISA antigen dose-response curve using ab32101 at 0~1000 ng/mL. Antigen concentration of 10 ng/mL. An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) (1/2500) was used as the secondary antibody.
This antibody preferentially recognizes phospho Y1007. When the concentration of peptides is lower than 10 ng/mL, it cannot recognize phospho Y1008.
-
Western blot - Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101)This image is courtesy of an anonymous AbreviewAll lanes : Anti-JAK2 (phospho Y1007 + Y1008) antibody [E132] (ab32101) at 1/2000 dilution
Lane 1 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 0 hours.
Lane 2 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 15 minutes.
Lane 3 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 30 minutes.
Lane 4 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 1 hour.
Lane 5 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 2 hours.
Lane 6 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 4 hours.
Lane 7 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 6 hours.
Lane 8 : Rat uterine cell line - whole cell lysate. Treated with 1µg/mL Prolactin for 24 hours.
Lysates/proteins at 30 µg per lane.
Secondary
All lanes : An HRP-conjugated donkey anti-rabbit polyclonal. at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 130 kDa
Observed band size: 110 kDa why is the actual band size different from the predicted?
Additional bands at: 55 kDa (possible non-specific binding)
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
-
SDS download
-
Datasheet download
文献 (209)
ab32101 被引用在 209 文献中.
- Fang J & Guan H γ-Secretase inhibitor alleviates lipopolysaccharide-induced myocardial injury through regulating JAK2/STAT3 signaling. Environ Toxicol 39:135-147 (2024). PubMed: 37671635
- Cai M et al. Fibroblast Growth Factor 21 Relieves Lipopolysaccharide-Induced Acute Lung Injury by Suppressing JAK2/STAT3 Signaling Pathway. Inflammation 47:209-226 (2024). PubMed: 37864659
- Shen L et al. Leptin secreted by adipocytes promotes EMT transition and endometrial cancer progression via the JAK2/STAT3 signalling pathway. Adipocyte 13:2293273 (2024). PubMed: 38090745
- Jiang X & Chen X Endometrial cell‑derived exosomes facilitate the development of adenomyosis via the IL‑6/JAK2/STAT3 pathway. Exp Ther Med 26:526 (2023). PubMed: 37869633
- Zheng LX et al. Curcumin alleviated dextran sulfate sodium-induced colitis by recovering memory Th/Tfh subset balance. World J Gastroenterol 29:5226-5239 (2023). PubMed: 37901446