产品: AMPK alpha 1 抗体
货号: AF6422
描述: Rabbit polyclonal antibody to AMPK alpha 1
应用: WB IHC IF/ICC
文献验证: WB, IHC
反应: Human, Mouse, Rat
预测: Zebrafish, Bovine, Sheep, Rabbit, Dog, Chicken, Xenopus
蛋白号: Q13131
RRID: AB_2835252

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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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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
克隆:
Polyclonal
特异性:
AMPK alpha 1 Antibody detects endogenous levels of total AMPK alpha 1.
RRID:
AB_2835252
引用格式: Affinity Biosciences Cat# AF6422, RRID:AB_2835252.
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

5 AMP activated protein kinase alpha 1catalytic subunit; 5 AMP activated protein kinase catalytic alpha 1 chain; 5' AMP activated protein kinase catalytic subunit alpha 1; 5'-AMP-activated protein kinase catalytic subunit alpha-1; AAPK1; AAPK1_HUMAN; ACACA kinase; acetyl CoA carboxylase kinase; AI194361; AI450832; AL024255; AMP -activate kinase alpha 1 subunit; AMP-activated protein kinase, catalytic, alpha -1; AMPK 1; AMPK alpha 1; AMPK alpha 1 chain; AMPK; AMPK subunit alpha-1; AMPK1; AMPKa1; AMPKalpha1; C130083N04Rik; cb116; EC 2.7.11.1; HMG CoA reductase kinase; HMGCR kinase; hormone sensitive lipase kinase; Hydroxymethylglutaryl CoA reductase kinase; im:7154392; kinase AMPK alpha1; MGC33776; MGC57364; OTTHUMP00000161795; OTTHUMP00000161796; PRKAA 1; PRKAA1; Protein kinase AMP activated alpha 1 catalytic subunit; SNF1-like protein AMPK; SNF1A; Tau protein kinase PRKAA1; wu:fa94c10;

抗原和靶标

免疫原:

A synthesized peptide derived from human AMPK alpha 1, corresponding to a region within C-terminal amino acids.

基因/基因ID:
描述:
AMPKA1 a protein kinase of the CAMKL family that plays a central role in regulating cellular and organismal energy balance in response to the balance between AMP/ATP, and intracellular Ca(2+) levels.

研究领域

· Cellular Processes > Transport and catabolism > Autophagy - animal.   (View pathway)

· Cellular Processes > Cellular community - eukaryotes > Tight junction.   (View pathway)

· Environmental Information Processing > Signal transduction > FoxO signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > mTOR signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > PI3K-Akt signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > AMPK signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Apelin signaling pathway.   (View pathway)

· Human Diseases > Endocrine and metabolic diseases > Insulin resistance.

· Human Diseases > Endocrine and metabolic diseases > Non-alcoholic fatty liver disease (NAFLD).

· Human Diseases > Cardiovascular diseases > Hypertrophic cardiomyopathy (HCM).

· Organismal Systems > Aging > Longevity regulating pathway.   (View pathway)

· Organismal Systems > Aging > Longevity regulating pathway - multiple species.   (View pathway)

· Organismal Systems > Environmental adaptation > Circadian rhythm.   (View pathway)

· Organismal Systems > Endocrine system > Insulin signaling pathway.   (View pathway)

· Organismal Systems > Endocrine system > Adipocytokine signaling pathway.

· Organismal Systems > Endocrine system > Oxytocin signaling pathway.

· Organismal Systems > Endocrine system > Glucagon signaling pathway.

文献引用

1). Strontium promotes osteogenic differentiation by activating autophagy via the the AMPK/mTOR signaling pathway in MC3T3‑E1 cells. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2019 (PubMed: 31173178) [IF=5.7]

Application: WB    Species: mouse    Sample: MC3T3‑E1 cells

Figure 6.| AMPK inhibition suppresses the effects of Sr. The MC3T3‑E1 cells were pre‑incubated with 5 µM compound C prior to osteogenic induction. (A‑E) Western blot analysis results for AMPK, p‑AMPK, LC‑3 I/II and OCN. Tubulin was used as an internal control. Quantitative analysis of AMPK, p‑AMPK, LC‑3 I/II and OCN is also shown, expressed as the means ± SD (n=3 for each group). **P<0.01; ***P<0.005; and ****P<0.001 compared with the control group. Sr, strontium chloride; AMPK, AMP‑activated protein kinase; LC, microtubule‑associated protein 1 light chain 3; OCN, osteocalcin.

2). Profile analysis and functional modeling identify circular RNAs in nonalcoholic fatty liver disease as regulators of hepatic lipid metabolism. Frontiers in genetics, 2022 (PubMed: 36186461) [IF=3.7]

Application: IHC    Species: mouse    Sample: hepatocytes

FIGURE 6. miR-466i-3p and miR-669c-3p activation induces AMPK-α1 downregulation and expressive promotion of lipogenic genes. (A,B) Both miR-466i-3p (A) and miR-669c-3p (B) targeted AMPK-α1 mRNA by the complementation of ‘seed sequence’ (miRNA) and 3′ untranslated region (mRNA). Triangles and circles labeling AMPK-α1 mRNA with serial numbers reflect the complementation sites of miR-466i-3p and miR-669c-3p, respectively. (C–E) miR-466i-3p and miR-669c-3p activation in the NAFLD group led to mRNA decrease in AMPK-α1 (C), whereas transcriptional increase in SREBP1 (D) and FASN (E). (F–I) Western blotting (F) semi-quantitatively confirmed the downregulation of AMPK-α1 (G) and upregulation of both SREBP1 (H) and FASN (I) in the NAFLD group. (J) Immunohistochemical staining revealed the expressive alterations of AMPK-α1, SREBP1, and FASN in hepatocytes. The data was presented as mean ± SEM. *, p < 0.05; **, p < 0.01; ***, p < 0.001.

Application: WB    Species: mouse    Sample: hepatocytes

FIGURE 6. miR-466i-3p and miR-669c-3p activation induces AMPK-α1 downregulation and expressive promotion of lipogenic genes. (A,B) Both miR-466i-3p (A) and miR-669c-3p (B) targeted AMPK-α1 mRNA by the complementation of ‘seed sequence’ (miRNA) and 3′ untranslated region (mRNA). Triangles and circles labeling AMPK-α1 mRNA with serial numbers reflect the complementation sites of miR-466i-3p and miR-669c-3p, respectively. (C–E) miR-466i-3p and miR-669c-3p activation in the NAFLD group led to mRNA decrease in AMPK-α1 (C), whereas transcriptional increase in SREBP1 (D) and FASN (E). (F–I) Western blotting (F) semi-quantitatively confirmed the downregulation of AMPK-α1 (G) and upregulation of both SREBP1 (H) and FASN (I) in the NAFLD group. (J) Immunohistochemical staining revealed the expressive alterations of AMPK-α1, SREBP1, and FASN in hepatocytes. The data was presented as mean ± SEM. *, p < 0.05; **, p < 0.01; ***, p < 0.001.

3). Liposomal Silybin Improves Glucose and Lipid Metabolisms in Type 2 Diabetes Mellitus Complicated with Non-Alcoholic Fatty Liver Disease via AMPK/TGF-β1/Smad Signaling. The Tohoku journal of experimental medicine, 2023 (PubMed: 37344419) [IF=1.7]

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