Product: Phospho-MSP/MST1 (Thr353) Antibody
Catalog: AF3688
Description: Rabbit polyclonal antibody to Phospho-MSP/MST1 (Thr353)
Application: WB
Cited expt.: WB
Reactivity: Human, Mouse, Rat
Mol.Wt.: 85kD; 80kD(Calculated).
Uniprot: P26927
RRID: AB_2847002

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Product Info

Source:
Rabbit
Application:
WB 1:500-1:2000
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

Reactivity:
Human,Mouse,Rat
Clonality:
Polyclonal
Specificity:
Phospho-MST1 (Thr353) Antibody detects endogenous levels of MST1 only when phosphorylated at Thr353.
RRID:
AB_2847002
Cite Format: Affinity Biosciences Cat# AF3688, RRID:AB_2847002.
Conjugate:
Unconjugated.
Purification:
The antibody is from purified rabbit serum by affinity purification via sequential chromatography on phospho-peptide and non-phospho-peptide affinity columns.
Storage:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias:

Fold/Unfold

D3F15S2; DNF15S2; Hepatocyte growth factor like protein alpha chain; Hepatocyte growth factor like protein; Hepatocyte growth factor like protein beta chain; Hepatocyte growth factor like protein homolog; Hepatocyte growth factor-like protein beta chain; HGFL; HGFL_HUMAN; Macrophage stimulating 1 (hepatocyte growth factor like); Macrophage stimulatory protein; Macrophage-stimulating protein; MSP; MST1; NF15S2; OTTHUMP00000208927;

Immunogens

Immunogen:

A synthesized peptide derived from human MST1 around the phosphorylation site of Thr353.

Uniprot:
Gene(ID):
Sequence:
MGWLPLLLLLTQCLGVPGQRSPLNDFQVLRGTELQHLLHAVVPGPWQEDVADAEECAGRCGPLMDCRAFHYNVSSHGCQLLPWTQHSPHTRLRRSGRCDLFQKKDYVRTCIMNNGVGYRGTMATTVGGLPCQAWSHKFPNDHKYTPTLRNGLEENFCRNPDGDPGGPWCYTTDPAVRFQSCGIKSCREAACVWCNGEEYRGAVDRTESGRECQRWDLQHPHQHPFEPGKFLDQGLDDNYCRNPDGSERPWCYTTDPQIEREFCDLPRCGSEAQPRQEATTVSCFRGKGEGYRGTANTTTAGVPCQRWDAQIPHQHRFTPEKYACKDLRENFCRNPDGSEAPWCFTLRPGMRAAFCYQIRRCTDDVRPQDCYHGAGEQYRGTVSKTRKGVQCQRWSAETPHKPQFTFTSEPHAQLEENFCRNPDGDSHGPWCYTMDPRTPFDYCALRRCADDQPPSILDPPDQVQFEKCGKRVDRLDQRRSKLRVVGGHPGNSPWTVSLRNRQGQHFCGGSLVKEQWILTARQCFSSCHMPLTGYEVWLGTLFQNPQHGEPSLQRVPVAKMVCGPSGSQLVLLKLERSVTLNQRVALICLPPEWYVVPPGTKCEIAGWGETKGTGNDTVLNVALLNVISNQECNIKHRGRVRESEMCTEGLLAPVGACEGDYGGPLACFTHNCWVLEGIIIPNRVCARSRWPAVFTRVSVFVDWIHKVMRLG

Research Backgrounds

PTMs:

Cleaved after Arg-483, probably by HPN/Hepsin, to yield the active form consisting of two disulfide-linked chains.

Subcellular Location:

Secreted.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
Family&Domains:

Belongs to the peptidase S1 family. Plasminogen subfamily.

References

1). Mechanical stretching can modify the papillary dermis pattern and papillary fibroblast characteristics during skin regeneration. Journal of Investigative Dermatology, 2022 (PubMed: 35181299) [IF=5.7]

Application: IF/ICC    Species: Rat    Sample:

Figure S2. Expanded rat skin was divided into well-regenerated and poorly regenerated groups, similar to regenerated human skin, and Fps were found to be widely distributed in both the upper papillary dermis and the lower reticular dermis. (a) Representative photographs of well-regenerated and poorly regenerated expanded rat skin. (b‒e) Histochemical assessments of (b, d) PCNA+ cells and (c, e) YAP+ cells in the rat dermis from the indicated groups and their quantification. n = 8. (f, g) Representative images showing DLK1 and LRIG1 costaining in (f) the papillary dermis and (g) the reticular dermis in each group. (h) LRIG1+ cells were widely distributed in the area surrounding the perifollicular dermis. The white dashed line shows hair follicles. (i) Representative images of TGFβ1 staining in the papillary dermis and the reticular dermis in each group. (j) Representative costained images of TGFβ1 and LRIG1 staining in well-regenerated rat skin. (k) Representative αSMA-stained images from each group. Bar = 100 μm. Data are presented as the mean ± SEM. One-way ANOVA followed by Tukey’s multiple comparison test was used. ∗P < 0.05, ∗∗P < 0.01. The results are representative of at least three independent experiments. CON denotes normal skin (control group), WELL denotes well-regenerated skin, POOR denotes poorly regenerated skin, and OLD denotes aged skin. αSMA, α-smooth muscle actin; Fp, papillary fibroblast; n.s., nonsignificant; PCNA, proliferating cell nuclear antigen.

2). Icariin regulates the Hippo/TAZ signaling pathway to promote osteogenic differentiation and bone remodeling in osteoporosis. Biochemical and biophysical research communications, 2025 (PubMed: 41264994) [IF=2.5]

Application: WB    Species: Rat    Sample: BMSCs

Fig. 3. Effect of ICA on Hippo signaling pathway in BMSCs (A- B) Relative mRNA expression levels of MST1 and TAZ (n = 3); (C–G) Relative protein expression levels of MST1, p-MST1, TAZ and p-TAZ (n = 3).

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