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ACTA1/α-actin Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
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  • 1 - ACTA1/α-actin Antibody (C-term) AW5259
    Western blot analysis of lysates from human placenta tissue lysate,RD cell line (from left to right), using ACTA1/α-actin Antibody (C-term)(Cat. #AW5259). AW5259 was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L(HRP) at 1:10000 dilution was used as the secondary antibody.
  • 14 - ACTA1/α-actin Antibody (C-term) AW5259
    ACTA1/α-actin Antibody (C-term) (AW5259)immunohistochemistry analysis in formalin fixed and paraffin embedded human skeletal muscle followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of ACTA1/α-actin Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.
  • 3 - ACTA1/α-actin Antibody (C-term) AW5259
    Confocal immunofluorescent analysis of ACTA1/α-actin Antibody (C-term)(Cat#AW5259) with A549 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green).DAPI was used to stain the cell nuclear (blue).
  • 4 - ACTA1/α-actin Antibody (C-term) AW5259
    ACTA1/α-actin Antibody (C-term) (Cat. #AW5259) flow cytometric analysis of CEM cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
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Product info
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
FC, IF, IHC-P
Primary Accession P68133
Other Accession P68136, P68135, P68137, P68134, P68139, P68138, P04751, P68035, P68033, P68032, P68034, Q3ZC07, P62738, P62740, P62737, P62736, P08023, P62739, P04752, P10995, NP_001091.1
Reactivity Human
Predicted Mouse, Rat, Rabbit, Chicken, Bovine, Xenopus
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Clone Names RB35391
Calculated MW H=42;M=42;Rat=42 KDa
Additional info
Gene ID 58
Other Names ACTA1; ACTA; Actin, alpha skeletal muscle; Alpha-actin-1
Target/Specificity This ACTA1/Alpha-actin antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 346-375 amino acids from the C-terminal region of human ACTA1/Alpha-actin.
Dilution WB~~1:1000
IHC-P~~1:10~50
IF~~1:10~50
FC~~1:10~50
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsACTA1/α-actin Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name ACTA1
Synonyms ACTA
Function Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
Cellular Location Cytoplasm, cytoskeleton.
Research Areas

BACKGROUND

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.

REFERENCES

Kim, E.Y., et al. Am. J. Physiol. Renal Physiol. 299 (3), F594-F604 (2010) :
Haigh, S.E., et al. Neuromuscul. Disord. 20(6):363-374(2010)
Yu, G., et al. J Clin Neurosci 17(6):766-769(2010)
Yu, C.H., et al. PLoS ONE 5 (7), E11878 (2010) :
Licastro, F., et al. Curr. Pharm. Des. 16(7):783-788(2010)

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