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AB81293

Anti-FAK (phospho Y861) 抗体 [EP841Y]

Anti-FAK (phospho Y861) antibody [EP841Y]

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(7 Publications)

Rabbit Recombinant Monoclonal FAK phospho Y861 antibody. Suitable for WB and reacts with Human, Mouse, Rat samples. Cited in 7 publications.

別名を表示する

FAK, FAK1, PTK2, Focal adhesion kinase 1, FADK 1, Focal adhesion kinase-related nonkinase, Protein phosphatase 1 regulatory subunit 71, Protein-tyrosine kinase 2, p125FAK, pp125FAK, FRNK, PPP1R71

3 Images
Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)
  • WB

Lab

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)

ab181602 was used as a GAPDH loading control.

All lanes:

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (ab81293) at 1/1000 dilution

Lane 1:

Untreated Jurkat (Human T cell leukemia T lymphocyte) whole cell lysate at 15 µg

Lane 2:

Jurkat treated with 10mM pervanadate for 30mins whole cell lysate at 15 µg

Lane 3:

Jurkat treated with 10mM pervanadate for 30mins whole cell lysate, then the membrane treated with phosphatase at 15 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Predicted band size: 119 kDa

false

Exposure time: 20s

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)
  • WB

Lab

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)

ab181602 was used as a GAPDH loading control.

All lanes:

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (ab81293) at 1/1000 dilution

Lane 1:

Untreated NIH/3T3 (Mouse embryonic fibroblast) whole cell lysate at 15 µg

Lane 2:

NIH/3T3 treated with 10mM pervanadate for 60mins whole cell lysate at 15 µg

Lane 3:

NIH/3T3 treated with 10mM pervanadate for 60mins whole cell lysate, then the membrane treated with phosphatase at 15 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Predicted band size: 119 kDa

false

Exposure time: 5s

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)
  • WB

Lab

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (AB81293)

ab181602 was used as a GAPDH loading control.

All lanes:

Western blot - Anti-FAK (phospho Y861) antibody [EP841Y] (ab81293) at 1/1000 dilution

Lane 1:

Untreated C6 (Rat glial tumor glial cell) whole cell lysate at 15 µg

Lane 2:

C6 treated with 10mM pervanadate for 60mins whole cell lysate at 15 µg

Lane 3:

C6 treated with 10mM pervanadate for 60mins whole cell lysate, then the membrane treated with phosphatase at 15 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Predicted band size: 119 kDa

false

Exposure time: 20s

関連する標識済み抗体及び組成の異なる製品 (1)

  • Carrier free

    Anti-FAK (phospho Y861) antibody [EP841Y] - BSA and Azide free

Key facts

宿主種

Rabbit

クローン性

Monoclonal

クローン番号

EP841Y

アイソタイプ

IgG

キャリアフリー

No

交差種

Mouse, Rat, Human

アプリケーション

WB

applications

免疫原

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "ICCIF" : {"fullname" : "Immunocytochemistry/ Immunofluorescence", "shortname":"ICC/IF"}, "IP" : {"fullname" : "Immunoprecipitation", "shortname":"IP"}, "FlowCyt" : {"fullname" : "Flow Cytometry", "shortname":"Flow Cyt"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "ICCIF-species-checked": "notRecommended", "ICCIF-species-dilution-info": "", "ICCIF-species-notes": "<p></p>", "IP-species-checked": "notRecommended", "IP-species-dilution-info": "", "IP-species-notes": "<p></p>", "FlowCyt-species-checked": "notRecommended", "FlowCyt-species-dilution-info": "", "FlowCyt-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/5000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "notRecommended", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" }, "Mouse": { "ICCIF-species-checked": "notRecommended", "ICCIF-species-dilution-info": "", "ICCIF-species-notes": "<p></p>", "IP-species-checked": "notRecommended", "IP-species-dilution-info": "", "IP-species-notes": "<p></p>", "FlowCyt-species-checked": "notRecommended", "FlowCyt-species-dilution-info": "", "FlowCyt-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/5000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "notRecommended", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" }, "Rat": { "ICCIF-species-checked": "notRecommended", "ICCIF-species-dilution-info": "", "ICCIF-species-notes": "<p></p>", "IP-species-checked": "notRecommended", "IP-species-dilution-info": "", "IP-species-notes": "<p></p>", "FlowCyt-species-checked": "notRecommended", "FlowCyt-species-dilution-info": "", "FlowCyt-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/5000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "notRecommended", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" } } }

製品の詳細

The production method for this product has been changed from hybridoma to recombinant on 15th April 2024.

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
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 batch production

For more information, read more on recombinant antibodies.

出荷温度及び保存条件

製品の状態
Liquid
精製方法
Affinity purification Protein A
バッファー組成
pH: 7.2 - 7.4 Preservative: 0.01% Sodium azide Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
出荷温度
Conditional Ambient
短期保存温度
+4°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Focal Adhesion Kinase (FAK) also known as Protein Tyrosine Kinase 2 (PTK2) is a non-receptor tyrosine kinase. This protein has a molecular weight of approximately 125 kDa. FAK is expressed at high levels in brain muscle and liver tissues. Mechanically FAK plays a role in cellular adhesion and migration by regulating integrin signaling and cell-extracellular matrix interactions. FAK auto-phosphorylates at tyrosine residue 397 creating a binding site for Src family kinases and promoting downstream signaling pathways.
Biological function summary

Focal Adhesion Kinase participates in the formation of focal adhesions which are complexes that connect the cytoskeleton to the extracellular matrix. The FAK protein functions as an important signaling node in these structures allowing for the assembly of multiprotein signal transduction complexes. FAK also controls cellular processes such as spreading motility and survival. The interaction with proteins such as Src kinases paxillin and talin facilitates its biological roles in cell signaling.

Pathways

Focal Adhesion Kinase engages in the regulation of the MAPK/ERK signaling pathway and the PI3K/AKT pathway. These pathways are instrumental for cell proliferation survival and migration. In these pathways FAK interacts with proteins such as PI3K Grb2 and Sos linking integrin-mediated signals with downstream effects that influence cell behavior and survival.

Altered FAK signaling has ties to cancer progression and metastasis as well as cardiovascular diseases. In cancer the overexpression of FAK and its interaction with proteins like Src and VEGFR can drive tumor growth and angiogenesis. In cardiovascular diseases improper FAK activation can lead to aberrant heart tissue remodeling and associated pathologies. Abnormalities in FAK signaling pathways can therefore contribute significantly to the development and progression of these diseases.

製品プロトコール

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ターゲットの情報

Non-receptor protein-tyrosine kinase that plays an essential role in regulating cell migration, adhesion, spreading, reorganization of the actin cytoskeleton, formation and disassembly of focal adhesions and cell protrusions, cell cycle progression, cell proliferation and apoptosis. Required for early embryonic development and placenta development. Required for embryonic angiogenesis, normal cardiomyocyte migration and proliferation, and normal heart development. Regulates axon growth and neuronal cell migration, axon branching and synapse formation; required for normal development of the nervous system. Plays a role in osteogenesis and differentiation of osteoblasts. Functions in integrin signal transduction, but also in signaling downstream of numerous growth factor receptors, G-protein coupled receptors (GPCR), EPHA2, netrin receptors and LDL receptors. Forms multisubunit signaling complexes with SRC and SRC family members upon activation; this leads to the phosphorylation of additional tyrosine residues, creating binding sites for scaffold proteins, effectors and substrates. Regulates numerous signaling pathways. Promotes activation of phosphatidylinositol 3-kinase and the AKT1 signaling cascade. Promotes activation of MAPK1/ERK2, MAPK3/ERK1 and the MAP kinase signaling cascade. Promotes localized and transient activation of guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs), and thereby modulates the activity of Rho family GTPases. Signaling via CAS family members mediates activation of RAC1. Phosphorylates NEDD9 following integrin stimulation (PubMed : 9360983). Recruits the ubiquitin ligase MDM2 to P53/TP53 in the nucleus, and thereby regulates P53/TP53 activity, P53/TP53 ubiquitination and proteasomal degradation. Phosphorylates SRC; this increases SRC kinase activity. Phosphorylates ACTN1, ARHGEF7, GRB7, RET and WASL. Promotes phosphorylation of PXN and STAT1; most likely PXN and STAT1 are phosphorylated by a SRC family kinase that is recruited to autophosphorylated PTK2/FAK1, rather than by PTK2/FAK1 itself. Promotes phosphorylation of BCAR1; GIT2 and SHC1; this requires both SRC and PTK2/FAK1. Promotes phosphorylation of BMX and PIK3R1. Isoform 6 (FRNK) does not contain a kinase domain and inhibits PTK2/FAK1 phosphorylation and signaling. Its enhanced expression can attenuate the nuclear accumulation of LPXN and limit its ability to enhance serum response factor (SRF)-dependent gene transcription.. Isoform 6. Isoform 6 (FRNK) does not contain a kinase domain and inhibits PTK2/FAK1 phosphorylation and signaling. Its enhanced expression can attenuate the nuclear accumulation of LPXN and limit its ability to enhance serum response factor (SRF)-dependent gene transcription.
See full target information PTK2 pY861

文献 (7)

Recent publications for all applications. Explore the full list and refine your search

Cancer cell international 25:191 PubMed40413506

2025

EphrinA2 promotes glioma cell migration and invasion through EphA2 and FAK.

Applications

Unspecified application

Species

Unspecified reactive species

Nozomi Hirai,Sho Tamai,Toshiya Ichinose,Hemragul Sabit,Norihiko Saito,Satoshi Iwabuchi,Mitsutoshi Nakada

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11:e2409081 PubMed39258781

2024

Enhanced Tumor-Targeted Delivery of Arginine-Rich Peptides via a Positive Feedback Loop Orchestrated by Piezo1/integrin β1 Signaling Axis.

Applications

Unspecified application

Species

Unspecified reactive species

Minghai Ma,Xing Li,Minxuan Jing,Pu Zhang,Mengzhao Zhang,Lu Wang,Xiao Liang,Yunzhong Jiang,Jianpeng Li,Jiale He,Xinyang Wang,Min Lin,Lei Wang,Jinhai Fan

Cell death & disease 11:972 PubMed33184263

2020

Exosome-derived ENO1 regulates integrin α6β4 expression and promotes hepatocellular carcinoma growth and metastasis.

Applications

Unspecified application

Species

Unspecified reactive species

Keqiu Jiang,Chengyong Dong,Zeli Yin,Rui Li,Jiakai Mao,Chengye Wang,Junlin Zhang,Zhenming Gao,Rui Liang,Qi Wang,Liming Wang

The Journal of pharmacy and pharmacology 70:1606-1618 PubMed30187481

2018

Bioinformatics analysis of microarray profiling identifies the mechanism of focal adhesion kinase signalling pathway in proliferation and apoptosis of breast cancer cells modulated by green tea polyphenol epigallocatechin 3-gallate.

Applications

Unspecified application

Species

Unspecified reactive species

Xiao Luo,Lihua Guo,Lirong Zhang,Yu Hu,Dongmei Shang,Degang Ji

Journal of immunology research 2018:4602570 PubMed29951557

2018

Integrin 9 Suppresses Hepatocellular Carcinoma Metastasis by Rho GTPase Signaling.

Applications

Unspecified application

Species

Unspecified reactive species

Yan-Li Zhang,Xin Xing,Li-Bo Cai,Lei Zhu,Xiao-Mei Yang,Ya-Hui Wang,Qin Yang,Hui-Zhen Nie,Zhi-Gang Zhang,Jun Li,Xue-Li Zhang

American journal of cancer research 7:531-542 PubMed28401009

2017

Integrin β1 is a critical effector in promoting metastasis and chemo-resistance of esophageal squamous cell carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Zhipeng Xu,Li Zou,Gang Ma,Xiaowei Wu,Furong Huang,Tingting Feng,Suqing Li,Qingfeng Lin,Xiaoting He,Zhihua Liu,Xiufeng Cao

Oncology letters 11:1889-1894 PubMed26998095

2016

AURKA promotes cell migration and invasion of head and neck squamous cell carcinoma through regulation of the AURKA/Akt/FAK signaling pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Jichang Wu,Liyun Yang,Yamin Shan,Changping Cai,Shili Wang,Hao Zhang
View all publications

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