Actb Rabbit Polyclonal Antibody [Clone ID: Poly6221]

SKU
TA328070
Rabbit Polyclonal anti-β-Actin Antibody
  $575.00
2 Weeks*
Bulk/Customize
Specifications
Specifications
Product Data
Clone Name Poly6221
Application IF, IHC, WB
Recommended Dilution WB, IF, IHC
Reactivity Human, Mouse, Rat
Antibody Host Rabbit
Isotype IgG
Clonality Polyclonal
Immunogen Peptide-KLH, NH2 terminus
Buffer This antibody is provided in phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 50% glycerol.
Purification The antibody was purified by affinity chromatography.
Conjugation Unconjugated
Storage Store at -20°C as received.
Stability Stable for 12 months from date of receipt.
Shipping Blue Ice
Predicted Protein Size 42 KD
Gene Name actin, beta
Database Link
Background β-actin is a ubiquitously expressed and highly conserved 42 kD cytoplasmic protein involved in cell motility. This critical cytoskeletal component can be disrupted by drugs such as cytochalasin. Because β-actin is ubiquitously expressed in all eukaryotic cells, it is frequently used as a loading control for assays involving protein detection (such as Western blotting). The Poly6221 antibody has been shown to be useful for Western blotting of mouse, rat, and human β-actin.
Synonyms Beta-actin; PS1TP5BP1
Reference Data
Protein Categories ADC Targets, Intracellular Proteins
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Documents
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file-alt Citations

Catalpol ameliorates intervertebral disc degeneration by suppressing NP cell Pyroptosis via the NF-ĸB pathway
Wang, Liang, Yang et al
Int Immunopharmacol (2026) 186, 117118 DOI: 10.1016/j.intimp.2026.117118
AI Summary: In this study, OriGene's GAPDH (TA802519) and β-ACTIN (TA328070) antibodies were used as loading controls in western blot experiments to validate protein expression levels during the investigation of catalpol's protective effects against intervertebral disc degeneration.
Snippet: P65 Rabbit 1:500 AF5006 Affinity Biosciencese GAPDH Mouse 1:20000 TA802519 OriGene β-ACTIN Mouse 1:20000 TA328070 OriGene
O-Sulfation disposition of curcumin and quercetin in SULT1A3 overexpressing HEK293 cells: the role of arylsulfatase B in cellular O-sulfation regulated by transporters
Pei, Dou, Zhang et al
Food Funct (2022)
Cited by 8
AI Summary: OriGene products—specifically the BCRP (TA322704), MRP4 (TA327332), and β-actin (TA328070) antibodies—were used in this study to detect and analyze transporter proteins involved in the O-sulfation and cellular excretion of curcumin and quercetin.
Snippet: BCRP (catalog number TA322704), MRP4 (catalog number TA327332), and β-actin (catalog number TA328070) were purchased from OriGene Technologies (Rockville, MD). …
Punicalagin Attenuates LPS-Induced Inflammation and ROS Production in Microglia by Inhibiting the MAPK/NF-κB Signaling Pathway and NLRP3 Inflammasome Activation
Lo, Liu, Li et al
J Inflamm Res (2022) 15, 5347-5359 DOI: 10.2147/JIR.S372773
AI Summary: In this study, the β-actin antibody (catalog number: TA328070) from OriGene was used as a loading control in Western blot experiments to assess protein expression changes in microglia treated with punicalagin.
Snippet: es were obtained from Santa Cruz Biotechnology (Dallas, TX, USA). NLRP3 (catalog number: GTX00763) and β-actin (catalog number: TA328070) antibodies were purchased from GeneTex (Irvine, CA, USA) and OriGene Technologies (Rockville, MD, USA) respectively. Cell Culture Mouse microglial BV2 cell line was obtained from the Food Industry Research and Development Institute (Hsinchu, Taiwan, R.O.C). Ce
FigureFigureFigure
WB
Regulatory effect between HMGA2 and the Wnt/β-catenin signaling pathway in the carcinogenesis of sporadic colorectal tubular adenoma
Li, Cao, Wang et al
Oncol Lett (2021) 22 (6), 849 DOI: 10.3892/ol.2021.13110
Cited by 7
AI Summary: OriGene's goat serum was used in this study to block non-specific binding sites during immunohistochemistry, contributing to the accurate detection of target proteins involved in the regulatory relationship between HMGA2 and the Wnt/β-catenin signaling pathway in colorectal tubular adenoma.
Snippet: antigen retrieval was performed with citrate buffer for 15 min at 120°C. Endogenous peroxidase activity was blocked using 3% hydrogen peroxide in methanol for 10 min at room temperature. Goat serum (OriGene Technologies, Inc.) was used for blocking non-specific binding sites for 1–2 h at room temperature. Slides were then incubated with primary antibodies against HMGA2 (1:300 dilution;GTX10051
FigureFigureFigure
IHC WB
Showing 1-4 of 4 papers.
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