Anti-Actin Antibody, Rabbit Polyclonal sinobiological 101273-T40

$86.00
In stock
SKU
101273-T40
Catalog No.SizePrice (USD)
101273-T40-2020 µL$88.87
101273-T40-5050 µL$147.96
101273-T40-100100 µL$251.64
101273-T40-200200 µL$355.32

General Information

Product nameAnti-Actin Antibody, Rabbit Polyclonal
Validated applicationsWB (FAQ Protocol), IHC-P (FAQ Protocol)
Species reactivityReacts with: Human, Mouse, Rat
SpecificityHuman, Mouse, Rat
ImmunogenA synthetic peptide corresponding to the N-terminus of the Human Actin
PreparationProduced in rabbits immunized with a synthetic peptide corresponding to the N-terminus of the Human Actin, and purified by antigen affinity chromatography.
SourcePolyclonal Rabbit IgG
PurificationProtein A & Antigen Affinity
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-ACTA Antibody; Anti-ASMA Antibody; Anti-CFTD Antibody; Anti-CFTD1 Antibody; Anti-CFTDM Antibody; Anti-CMYP2A Antibody; Anti-CMYP2B Antibody; Anti-CMYP2C Antibody; Anti-MPFD Antibody; Anti-NEM1 Antibody; Anti-NEM2 Antibody; Anti-NEM3 Antibody; Anti-SHPM Antibody

Image / Experimental Information

Image 1 DescriptionAnti-ACTA1 rabbit polyclonal antibody at 1:500 dilution Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:42 kDa Observed band size:45 kDa
Image 1 Alt TextHuman Actin Western blot (WB) 19393
Image 1 URLSource image
Image 2 DescriptionAnti-ACTA1 rabbit polyclonal antibody at 1:500 dilution Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:42 kDa Observed band size:45 kDa
Image 2 Alt TextHuman Actin Immunohistochemistry(IHC) 19394
Image 2 URLSource image
Image 3 DescriptionAnti-ACTA1 rabbit polyclonal antibody at 1:500 dilution Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:42 kDa Observed band size:45 kDa
Image 3 Alt TextHuman Actin Immunohistochemistry(IHC) 19395
Image 3 URLSource image
Image 4 DescriptionAnti-ACTA1 rabbit polyclonal antibody at 1:500 dilution Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:42 kDa Observed band size:45 kDa
Image 4 Alt TextHuman Actin Immunohistochemistry(IHC) 19396
Image 4 URLSource image
Image 5 DescriptionAnti-ACTA1 rabbit polyclonal antibody at 1:500 dilution Lane A: Hela Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:42 kDa Observed band size:45 kDa
Image 5 Alt TextHuman Actin Immunohistochemistry(IHC) 19397
Image 5 URLSource image

Background Information

Full Nameactin, alpha 1, skeletal muscle
DescriptionNemaline myopathy (NM) is one of the most common congenital nondystrophic myopathies and is characterized by muscle weakness, often from birth. Mutations in ACTA1 are a frequent cause of NM (ie, NEM3). ACTA1 encodes alpha-actin 1, the main constituent of the sarcomeric thin filament. The mechanisms by which mutations in ACTA1 contribute to muscle weakness in NEM3 are incompletely understood. Mutations in skeletal muscle α-actin 1-encoding gene (ACTA1) cause autosomal dominant or recessive myopathies with marked clinical and pathological heterogeneity. Patients typically develop generalized or limb-girdle pattern of weakness, that clinically severe ACTA1-related myopathy can present with muscle morphological findings suggestive of cytoplasmic body myopathy in the absence of definite nemaline rods. The Asn94Lys mutation in skeletal muscle sarcomeric α-actin may be linked to this histological appearance.

title: Ultrathin BSA-Stabilized Black Phosphorous Nanoreactor Boosts Mild-Temperature Photothermal Therapy Through Modulation of Cellular Self-Defense Fate.
authors: Guoping Jia; Qinghe Wu; ...; Chunfu Zhang
journal: Advanced Healthcare Materials
date: 2024-12-17
pmid: 39225409
doi: 10.1002/adhm.202402079
cited_by_count: 6
techniques: CCK-8 Assay; Cell Culture; Purification
bioz_score: 92

title: Chlorogenic acid inhibits the proliferation of human lung cancer A549 cell lines by targeting annexin A2 in vitro and in vivo.
authors: Lei Wang; Hongwu Du; Peng Chen
journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
date: 2021-02-18
pmid: 32882585
doi: 10.1016/j.biopha.2020.110673
cited_by_count: 80
techniques: Enzyme-linked Immunosorbent Assay; Imaging; Incubation; Membrane; SDS Page; Western Blot
bioz_score: 92

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