ab11597 AMPK alpha 1 Antibody

Western blot analysis of extracts from Mouse brain, using AMPK alpha 1 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of extracts from Mouse testis, using AMPK1 Antibody. The lane on the left was treated with blocking peptide. Observed bands: 70 kDa.
Western blot analysis of extracts from various samples, using AMPK1 Antibody. Lane 1: Mouse liver lysates; Lane 2: Rat liver lysates; Lane 3: Rat liver lysates treated with blocking peptide;
Western blot analysis of extracts from Mouse muscle, using AMPK1 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of extracts from various samples, using AMPK1 Antibody. Lane 1: RAW264.7 cells, blocked with antigen-specific peptides, Lane 2: RAW264.7 cells, Lane 3: EC304 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.

品牌

产品货号

ab11597

来源种属

Rabbit

抗体克隆

Polyclonal

来源亚型

IgG

实验方法

WB,IHC,IF,ICC

实验种属

Human,Mouse,Rat,Rabbit,Pig,Dog,Chicken,Bovine,Horse,Sheep

偶联标记

Unconjugated

目的蛋白

AMPK alpha 1

产品规格

50μl,100μl,200μl

产品报价

¥1500/¥2750/¥3600

实验应用


Western blotting

Recommended dilution: 1:500-1:2000


Immunofluorescence

Recommended dilution: 1:100-1:500


immunocytochemistry

Recommended dilution: 1:100-1:500


Immunohistochemistry

Recommended dilution: 1:50-1:200




最佳稀释倍数与浓度应由实验研究人员确认

产品说明



产品背景

Catalytic subunit of AMP-activated protein kinase (AMPK), an energy sensor protein kinase that plays a key role in regulating cellular energy metabolism. In response to reduction of intracellular ATP levels, AMPK activates energy-producing pathways and inhibits energy-consuming processes: inhibits protein, carbohydrate and lipid biosynthesis, as well as cell growth and proliferation. AMPK acts via direct phosphorylation of metabolic enzymes, and by longer-term effects via phosphorylation of transcription regulators. Also acts as a regulator of cellular polarity by remodeling the actin cytoskeleton; probably by indirectly activating myosin. Regulates lipid synthesis by phosphorylating and inactivating lipid metabolic enzymes such as ACACA, ACACB, GYS1, HMGCR and LIPE; regulates fatty acid and cholesterol synthesis by phosphorylating acetyl-CoA carboxylase (ACACA and ACACB) and hormone-sensitive lipase (LIPE) enzymes, respectively. Regulates insulin-signaling and glycolysis by phosphorylating IRS1, PFKFB2 and PFKFB3. AMPK stimulates glucose uptake in muscle by increasing the translocation of the glucose transporter SLC2A4/GLUT4 to the plasma membrane, possibly by mediating phosphorylation of TBC1D4/AS160. Regulates transcription and chromatin structure by phosphorylating transcription regulators involved in energy metabolism such as CRTC2/TORC2, FOXO3, histone H2B, HDAC5, MEF2C, MLXIPL/ChREBP, EP300, HNF4A, p53/TP53, SREBF1, SREBF2 and PPARGC1A. Acts as a key regulator of glucose homeostasis in liver by phosphorylating CRTC2/TORC2, leading to CRTC2/TORC2 sequestration in the cytoplasm. In response to stress, phosphorylates 'Ser-36' of histone H2B (H2BS36ph), leading to promote transcription. Acts as a key regulator of cell growth and proliferation by phosphorylating TSC2, RPTOR and ATG1/ULK1: in response to nutrient limitation, negatively regulates the mTORC1 complex by phosphorylating RPTOR component of the mTORC1 complex and by phosphorylating and activating TSC2. In response to nutrient limitation, promotes autophagy by phosphorylating and activating ATG1/ULK1. In that process also activates WDR45. In response to nutrient limitation, phosphorylates transcription factor FOXO3 promoting FOXO3 mitochondrial import (By similarity). AMPK also acts as a regulator of circadian rhythm by mediating phosphorylation of CRY1, leading to destabilize it. May regulate the Wnt signaling pathway by phosphorylating CTNNB1, leading to stabilize it. Also has tau-protein kinase activity: in response to amyloid beta A4 protein (APP) exposure, activated by CAMKK2, leading to phosphorylation of MAPT/TAU; however the relevance of such data remains unclear in vivo. Also phosphorylates CFTR, EEF2K, KLC1, NOS3 and SLC12A1.

Description
Rabbit polyclonal antibody to AMPK alpha 1

Applications 
WB, IF, ICC, IHC.

Immunogen 
AMPK alpha 1 Antibody detects endogenous levels of total AMPK alpha 1.

Reactivity 
Human, Mouse, Rat.
可预测:Zebrafish(82%), Bovine(%), Sheep(%), Rabbit(%), Dog(%), Chicken(%), Xenopus(%)

Molecular weight
62kDa, 70 kDa; 64kD(Calculated).

Host species 
Rabbit

Ig class 
Immunogen-specific rabbit IgG

Purification 
Antigen affinity purification

Full name 
AMPK alpha 1

Synonyms 
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;

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.

Swissprot 
Q13131

产品图片

Western blot analysis of extracts from Mouse brain, using AMPK alpha 1 Antibody. The lane on the left was treated with blocking peptide.

Western blot analysis of extracts from Mouse testis, using AMPK1 Antibody. The lane on the left was treated with blocking peptide. Observed bands: 70 kDa.

Western blot analysis of extracts from various samples, using AMPK1 Antibody. Lane 1: Mouse liver lysates; Lane 2: Rat liver lysates; Lane 3: Rat liver lysates treated with blocking peptide;

Western blot analysis of extracts from Mouse muscle, using AMPK1 Antibody. The lane on the left was treated with blocking peptide.

Western blot analysis of extracts from various samples, using AMPK1 Antibody. Lane 1: RAW264.7 cells, blocked with antigen-specific peptides, Lane 2: RAW264.7 cells, Lane 3: EC304 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.

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