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F9176

Sigma-Aldrich

Anti-phospho-FAK (pTyr861) antibody produced in rabbit

affinity isolated antibody, buffered aqueous glycerol solution

Synonym(s):

Anti-phospho-Focal Adhesion Kinase

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.44

biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous glycerol solution

species reactivity

frog, chicken, human, mouse

technique(s)

immunohistochemistry: suitable
western blot: 1:1,000

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

phosphorylation (pTyr861)

Gene Information

human ... PTK2(5747)
mouse ... Ptk2(14083)

General description

Focal adhesion kinase (FAK) is a cytoplasmic protein that belongs to non-receptor protein tyrosine kinase family. It has a critical role in regulation of cell differentiation, migration, adhesion and acceleration of the G1 to S phase transition in cell cycle. Anti-phospho-FAK (pTyr861) antibody can be used in immunohistochemistry. Rabbit anti-phospho-FAK (pTyr861) antibody reacts specifically with FAK (125kD) phosphorylated at tyrosine 861. This product can also react with FAK (pTyr861) of mouse, chicken and human.
Focal adhesion kinase (FAK) is a non-receptor cytoplasmic protein tyrosine kinase. It is coded by the PTK2 (protein tyrosine kinase 2) gene that is located on human chromosome 8q24.3.

Immunogen

synthetic phosphopeptide derived from the region of FAK that contains tyrosine 861.

Application

Anti-phospho-FAK (pTyr861) antibody can be used in western blotting (diluted 1:1000).

Biochem/physiol Actions

Focal adhesion kinase (FAK) participates in cell signaling pathways that leads to cell proliferation, invasion, survival and metastasis. It is essential for normal embryonic development. This protein controls CSC (cancer stem cells) properties in breast, gastrointestinal and squamous cell carcinoma.

Physical form

Solution in Dulbecco′s phosphate buffered saline (without Mg2+ and Ca2+), pH 7.3, with 50% glycerol, 1.0 mg/ml BSA (IgG and protease free) and 0.05% sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

含少量动物源组分生物产品
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Chifumi Ohyagi-Hara et al.
The American journal of pathology, 182(5), 1876-1889 (2013-03-19)
Ovarian cancer is characterized by widespread peritoneal dissemination and ascites and has a cure rate of only 30%. As has been previously reported, integrin α5 plays a key role in the peritoneal dissemination of ovarian cancer. Our aim was to
Potential roles for focal adhesion kinase in development.
Ridyard MS, Sanders EJ
Anat. Embryol., 199(1), 1-7 (1999)
J D Owen et al.
Molecular and cellular biology, 19(7), 4806-4818 (1999-06-22)
Focal adhesion kinase (FAK) is a nonreceptor protein tyrosine kinase involved in integrin-mediated control of cell behavior. Following cell adhesion to components of the extracellular matrix, FAK becomes phosphorylated at multiple sites, including tyrosines 397, 576, and 577. Tyr-397 is
Hua-Li Yu et al.
International journal of molecular sciences, 25(13) (2024-07-13)
Microglia migrate to the cerebral cortex during early embryonic stages. However, the precise mechanisms underlying microglia migration remain incompletely understood. As an extracellular matrix protein, Netrin-1 is involved in modulating the motility of diverse cells. In this paper, we found
Adrian Krajewski et al.
Cancer management and research, 12, 13085-13097 (2020-12-31)
Cyclins are well-known cell cycle regulators. The activation of cyclin-dependent kinases by cyclins allows orchestration of the complicated cell cycle machinery and drives the cell from the G1 phase to the end of the mitotic phase. In recent years, it

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