S100A4 Antibody - #DF6516

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产品: S100A4 抗体
货号: DF6516
描述: Rabbit polyclonal antibody to S100A4
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Bovine, Horse, Rabbit, Dog
分子量: 12kDa; 12kD(Calculated).
蛋白号: P26447
RRID: AB_2838478

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   规格 价格 库存
 50ul RMB¥ 1250 现货
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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MSDS
说明书
COA
实验方案
WB Handbook
IHC Protocol
IF/ICC Protocol

产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Mouse,Rat
预测:
Pig(100%), Bovine(100%), Horse(100%), Rabbit(100%), Dog(100%)
克隆:
Polyclonal
特异性:
S100A4 Antibody detects endogenous levels of total S100A4.
RRID:
AB_2838478
引用格式: Affinity Biosciences Cat# DF6516, RRID:AB_2838478.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
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.
别名:

展开/折叠

18A2; 42A; calcium Placental protein; Calvasculin; CAPL; Fibroblast specific protein 1 (FSP1); Fibroblast specific protein 1; Fibroblast specific protein; FSP1; Leukemia multidrug resistance associated protein; Malignant transformation suppression 1 (MTS1); Malignant transformation suppression 1; Metastasin; MTS1; OTTHUMP00000015467; OTTHUMP00000015468; P9KA; PEL98; Placental calcium-binding protein; Protein Mts1; Protein S100 A4; Protein S100-A4; S100 calcium binding protein A4 (calcium protein, calvasculin, metastasin, murine placental homolog); S100 calcium binding protein A4; S100 calcium-binding protein A4; S100a4; S10A4_HUMAN;

抗原和靶标

免疫原:
Uniprot:

P26447(S10A4_HUMAN) >>Visit HPA database.

基因/基因ID:
S100A4(6275)
表达:
P26447 S10A4_HUMAN:

Ubiquitously expressed.

描述:
The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in motility, invasion, and tubulin polymerization. Chromosomal rearrangements and altered expression of this gene have been implicated in tumor metastasis. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
序列:
MACPLEKALDVMVSTFHKYSGKEGDKFKLNKSELKELLTRELPSFLGKRTDEAAFQKLMSNLDSNRDNEVDFQEYCVFLSCIAMMCNEFFEGFPDKQPRKK

种属预测

种属预测:

score>80的预测可信度较高，可尝试用于WB检测。*预测模型主要基于免疫原序列比对，结果仅作参考，不作为质保凭据。

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Dog
100
Rabbit
100
Sheep
0
Xenopus
0
Zebrafish
0
Chicken
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - P26447 作为底物

Site PTM Type Enzyme
M1 Acetylation
K7 Acetylation
K18 Acetylation
K18 Ubiquitination
K22 Sumoylation
K22 Ubiquitination
K28 Sumoylation
K31 Acetylation
K31 Sumoylation
K31 Ubiquitination
S32 Phosphorylation
K35 Acetylation
K35 Ubiquitination
S44 Phosphorylation
K48 Acetylation
K48 Ubiquitination
K57 Acetylation
K57 Ubiquitination
S64 Phosphorylation
K96 Sumoylation
K96 Ubiquitination

研究背景

组织特异性:

Ubiquitously expressed.

亚基结构:

Homodimer. Interacts with PPFIBP1 in a calcium-dependent mode.

蛋白家族:

Belongs to the S-100 family.

文献引用

1). Exosomal miR-500a-5p derived from cancer-associated fibroblasts promotes breast cancer cell proliferation and metastasis through targeting USP28. Theranostics, 2023 (PubMed: 33664871) [IF=12.4]
2). Long-Term Administration of Triterpenoids From Ganoderma lucidum Mitigates Age-Associated Brain Physiological Decline via Regulating Sphingolipid Metabolism and Enhancing Autophagy in Mice. Frontiers in Aging Neuroscience, 2021 (PubMed: 34025387) [IF=4.8]

Application: WB    Species: Mice    Sample: liver and spleen tissue

FIGURE 6 Improvement of multiple organ aging after long-term administration of TGL. TGL shows an improvement in the liver and spleen. (A) TGL shows inhibition of the expressions in mTOR and p-mTOR of the liver. (B) The expression of GPX4 and S100A4. (C) TGL shows inhibition of telomere shortening in the liver. Data are presented as the means ± SD of more than six independent experiments and more than three independent experiments in Western blot. *p < 0.05, **p < 0.01, ***p < 0.001, and ns, not statistically significant.

Application: WB    Species: mouse    Sample: liver

FIGURE 6 | Improvement of multiple organ aging after long-term administration of TGL. TGL shows an improvement in the liver and spleen.(C) TGL shows inhibition of telomere shortening in the liver. Data are presented as the means ± SD of more than six independent experiments and more than three independent experiments in Western blot.
3). Regulation of cardiac fibroblasts reprogramming into cardiomyocyte-like cells with a cocktail of small molecule compounds. FEBS open bio, 2024 (PubMed: 38693086) [IF=2.6]

Application: IF/ICC    Species: Rat    Sample: cardiac fibroblasts

Fig. 1 Morphology and identification of cardiac fibroblasts (CFs) with Vimentin, discoidin domain receptor 2 (DDR2), and fibroblasts specific protein1 (FSP1). (A) Morphology of CFs by phase‐contrast imaging. (B) Colocalization of Vimentin and DDR2 on passage 3 of CF detected by immunofluorescence assays. (C) Colocalization of FSP1 and DDR2 on passage 3 of CF detected by immunofluorescence assays. Scale bars: 100 μm. (D) Statistics of positive expression rates of Vimentin, FSP1, and DDR2. The difference was assayed using one‐way ANOVA with the Tukey–Kramer posttest. Data are presented as the mean ± SEM; n = 3.
4). Suppression of ADAM8 attenuates angiotensin II-induced cardiac fibrosis and endothelial-mesenchymal transition via inhibiting TGF-β1/Smad2/Smad3 pathways. EXPERIMENTAL ANIMALS, 2022 (PubMed: 34615811) [IF=2.4]

Application: WB    Species: Mouse    Sample: heart endothelial cells

Fig. 4. ADAM8 silencing suppresses Ang II-induced EndMT in vivo. (A) Representative western blot bands of α-SMA, FSP1 and VE-cadherin were displayed. (B-D) The quantitative analysis of α-SMA, FSP1 and VE-cadherin was showed. *P<0.05, ***P<0.001 and ****P<0.0001. Multiple comparisons were performed using one-way ANOVA followed by Bonferroni’s post hoc test.

Application: IF/ICC    Species: Mouse    Sample: heart endothelial cells

Fig. 6. ADAM8 inhibition ameliorated Ang II-induced EndMT in vitro. (A) Primary mouse heart endothelial cells. (B) The purity of endothelial cells was measured via flow cytometry. (C, D) The endothelial cells were infected with lentivirus-shRNA targeting ADAM8. Lentivirus infection efficiency was detected via real-time PCR and western blot. (E-G) The EndMT-related makers, α-SMA, FSP1 and VE-cadherin, were determined by real-time PCR. (H) Endothelial cells were co-immunostained to detect CD31 (green) and FSP-1 (red). **P<0.01, ***P<0.001 and ****P<0.0001. Multiple comparisons were performed using one-way ANOVA followed by Bonferroni’s post hoc test.
5). Downregulation of acylglycerol kinase suppresses high glucose-induced endothelial-mesenchymal transition in HRECs through regulating the LPAR1/TGF-β/Notch signaling pathway. CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2021 (PubMed: 34559978) [IF=2.1]

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