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内参抗体
Rabbit Anti-beta-Actin (Loading Control) antibody
多克隆  |   SKU:bs-0061R

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货号:bs-3351R
¥1280
订购号:bs-0061R
¥680.00-4000.00
货期:现货
Rabbit Anti-beta-Actin (Loading Control) antibody
反应物种(预测)

Chicken,Dog,Pig,Rabbit,Sheep,Bee,Fish,GuineaPig,Hamster,Cat

产品应用(已验证)

WB,ICC,FCM,ELISA

产品应用(可尝试)

IHC

推荐稀释比例

WB=1:5000-50000,Elisa=1:5000-20000,IHC-P=1:500-1000,Flow Cyt=1μg/Test,ICC=1:100,

研究领域

肿瘤,细胞生物,信号转导,细胞骨架,

标签

Array

  • Sample:
    A549 Cell (Human) Lysate at 30 ug
    Primary: Lane1: Anti-beta-Actin (bs-0061R) at 1/500 dilution
    Lane2: Anti-beta-Actin (bs-0061R) at 1/1000 dilution
    Lane3: Anti-beta-Actin (bs-0061R) at 1/2000 dilution
    Lane4: Anti-beta-Actin (bs-0061R) at 1/4000 dilution
    Lane5: Anti-beta-Actin (bs-0061R) at 1/5000 dilution
    Lane6: Anti-beta-Actin (bs-0061R) at 1/8000 dilution
    Lane7: Anti-beta-Actin (bs-0061R) at 1/10000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Tissue/cell: Hela cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (beta-Actin) polyclonal Antibody, Unconjugated (bs-0061R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG-FITC antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.
  • Blank control:Mouse spleen.
    Primary Antibody (green line): Rabbit Anti-beta-Actin (Loading Control) antibody (bs-0061R)
    Dilution: 2μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-AF647
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at-20℃. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
  • Blank control: NIH/3T3.
    Primary Antibody (green line): Rabbit Anti-beta-Actin (Loading Control) antibody (bs-0061R)
    Dilution: 1μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-AF488
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at -20℃. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
  • Sample:
    Thymus (Mouse) Lysate at 40 ug
    Primary:
    Anti-beta-Actin (bs-0061R) at 1/1000~1/20000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Sample:
    SH-SY5Y (Human) Lysate at 40 ug
    Primary:
    Anti-beta-Actin (bs-0061R) at 1/2000~1/20000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Sample: Lung lysate at 30ug;
    Primary: Anti-beta-actin (bs-0061R) at 1:1000 dilution
    Secondary: HRP conjugated Goat-Anti-Rabbit IgG(bse-0295G) at 1:3000 dilution
    Predicted band size : 42kD
    Observed band size : 42kD
  • Tissue/cell: human cervical carcinoma; 4% Paraformaldehyde-fixed and paraffin-embedded;
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
    Incubation: Anti-Beta-actin Polyclonal Antibody, Unconjugated(bs-0061R) 1:1500, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
  • Blank control: RSC96(blue).
    Primary Antibody: Rabbit Anti-beta-Actin /FITC Conjugated antibody (bs-0061R/FITC), Dilution: 1μg in 100 μL 1X PBS containing 0.5% BSA;
    Isotype Control Antibody: Rabbit IgG/FITC(orange) ,used under the same conditions.
    Protocol
    The cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with ice-cold 90% methanol for 30 min on ice. The cells were washed twice with 1 X PBS. The cells were incubated in 1 X PBS containing 0.5% BSA + 1 0% goat serum (15 min) to block non-specific protein-protein interactions followed by the incubated with antibody (bs-0061R/FITC, 1μg /1x10^6 cells) for 30 min on ice. Acquisition of 20,000 events was performed.
  • Sample:
    Lane1: 293T Cell Lysate at 25 ug
    Lane2: A549 Cell Lysate at 25 ug
    Lane3: A431 Cell Lysate at 25 ug
    Primary: Anti- beta-Actin (bs-0061R) at 1/1000 and 1/5000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42kD
    Observed band size: 42 kD
  • Sample:
    A549 (Human) Cell Lysate at 40 ug
    Raw264.7 (Mouse) Cell Lysate at 40 ug
    SH-SY5Y (Human) Cell Lysate at 40 ug
    MKN45 (Human) Cell Lysate at 40 ug
    CHO (Human) Cell Lysate at 40 ug
    Panc-1 (Human) Cell Lysate at 40 ug
    4T1 (Human) Cell Lysate at 40 ug
    ASPC-1 (Human) Cell Lysate at 40 ug
    H9C2 (Rat) Cell Lysate at 40 ug
    Brl-3a (Rat) Cell Lysate at 40 ug
    TT (Human) Cell Lysate at 40 ug
    TEV-1 (Human) Cell Lysate at 40 ug
    EC9706 (Human) Cell Lysate at 40 ug
    Primary: Anti-beta-Actin (bs-0061R) at 1/2000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Sample:
    HL60 (Human) Cell Lysate at 40 ug
    HUVEC (Human) Cell Lysate at 40 ug
    Spinal cord (Rat) Lysate at 40 ug
    Rectum (Rat) Lysate at 40 ug
    Placenta (Rat) Lysate at 40 ug
    Lymph node (Rat) Lysate at 40 ug
    Lung (Rat) Lysate at 40 ug
    Spleen (Rat) Lysate at 40 ug
    JAR (Human) Cell Lysate at 40 ug
    293T (Human) Cell Lysate at 40 ug
    Jurkat (Human) Cell Lysate at 40 ug
    TM4 (Human) Cell Lysate at 40 ug
    Primary: Anti-beta-Actin (bs-0061R) at 1/2000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Sample:
    Thymus (Mouse) Lysate at 40 ug
    Urinary bladder (Mouse) Lysate at 40 ug
    Uterus (Mouse) Cell Lysate at 40 ug
    Aorta (Mouse) Lysate at 40 ug
    olfactory bulb (Mouse) Lysate at 40 ug
    Cerebellum (Mouse) Lysate at 40 ug
    Adrenal gland (Mouse) Lysate at 40 ug
    Ovary (Mouse) Lysate at 40 ug
    Ear (Mouse) Lysate at 40 ug
    U2os (Human) Cell Lysate at 40 ug
    ASPC-1 (Human) Cell Lysate at 40 ug
    Vas deferens (Mouse) Lysate at 40 ug
    trachea (Mouse) Lysate at 40 ug
    Primary: Anti-beta-Actin (bs-0061R) at 1/2000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • Sample:
    Embryo Cerebrum (Mouse) Lysate at 40 ug
    Du145 (Human) Lysate at 40 ug
    SW480 (Human) Cell Lysate at 40 ug
    U87MG (Human) Lysate at 40 ug
    U251 (Human) Lysate at 40 ug
    A673 (Human) Lysate at 40 ug
    Lovo (Human) Lysate at 40 ug
    293FT (Human) Lysate at 40 ug
    JEG-3 (Human) Lysate at 40 ug
    RSC96 (Rat) Cell Lysate at 40 ug
    MCF-7 (Human) Cell Lysate at 40 ug
    HepG2 (Human) Lysate at 40 ug
    A431 (Human) Lysate at 40 ug
    Primary: Anti-beta-Actin (bs-0061R) at 1/2000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 42 kD
  • MCF7 cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (beta-Actin) polyclonal Antibody, Unconjugated (bs-0061R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.
  • MCF7 cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (beta-Actin) polyclonal Antibody, Unconjugated (bs-0061R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.

产品信息

RRID:AB_10855480
产品名称:Rabbit Anti-beta-Actin (Loading Control) antibody
别名: Beta Actin; beta-Actin; ACTB; Actin cytoplasmic 1; Actin, beta; Beta actin; beta cytoskeletal actin; A X actin like protein; ACTB; Actin cytoplasmic 1; alpha sarcomeric Actin; Actx; Beta cytoskeletal actin; Melanoma X actin; PS1TP5BP1; ACTB_HUMAN.
中文名称:β-肌动蛋白/β-Actin(内参)抗体1
英文名称:Rabbit Anti-beta-Actin (Loading Control) antibody
中文别名:β actin; βactin;
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞浆
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

免疫原信息

免 疫 原:Synthetic MAP peptide derived from human beta-Actin
抗原表位:1-200/375
SWISS:P60709
Gene ID :60
Human Gene ID:60

产品介绍

Loading Control
This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, and integrity. This actin is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins. [provided by RefSeq, Jul 2008].
Function:Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
Subunit:Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others. Identified in a mRNP granule complex, at least composed of ACTB, ACTN4, DHX9, ERG, HNRNPA1, HNRNPA2B
Subcellular Location:Cytoplasm. cytoskeleton.
Tissue Specificity:Ubiquitously expressed in all eukaryotic cells.
Post-translational modifications:ISGylated.
Oxidation of Met-44 by MICALs (MICAL1, MICAL2 or MICAL3) to form methionine sulfoxide promotes actin filament depolymerization. Methionine sulfoxide is produced stereospecifically, but it is not known whether the (S)-S-oxide or the (R)-S-oxi
DISEASE:Defects in ACTA1 are the cause of nemaline myopathy type 3 (NEM3) [MIM:161800]. A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-or rod-like structu
Similarity:Belongs to the actin family.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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