bs-0159R [Primary Antibody]
Rabbit  Anti-Tubulin-alpha (Loading Control)  Polyclonal Antibody
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Host: Rabbit

Target Protein: Tubulin-alpha (Loading Control)

IR: Immunogen Range:375-448/448

Clonality: Polyclonal

Isotype: IgG

Entrez Gene: 7846

Swiss Prot: Q71U36

Source: KLH conjugated synthetic peptide derived from human Tubulin-alpha 1:375-448/448 

Purification: affinity purified by Protein A

Storage: 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Background: Tubulin is a major cytoskeleton that has five distinct forms, designated alpha, beta, gamma, delta and epsilon tubulin. The alpha and beta tubulins form a heterodimer that polymerize into the cylindrical microtubule fibers. Both alpha and beta tubulin bind GTP. Only beta tubulin hydrolyzes GTP to GDP. This hydrolysis is a process that is linked to tubulin polymerization and microtubule formation. The alpha tubulin isomer can be modified by addition of a C-terminal tyrosine residue. This modification may influence polymerization rates. The gamma tubulin isomer is localized to centrosomes which compose the heart of the microtubule organizing center from which microtubule fibers emanate.

Size: 50ul

Concentration: 1mg/ml

Applications: WB=1:2000-5000,Flow-Cyt=1μg/Test,ELISA=1:5000-10000

Cross Reactive Species: Human,Mouse,Rat (predicted: Sheep,Cow)

For research use only. Not intended for diagnostic or therapeutic use.

VALIDATION IMAGES
Sample: Lane 1: Human HeLa cell lysates Lane 2: Human Jurkat cell lysates Lane 3: Human SH-SY5Y cell lysates Lane 4: Human U-2 OS cell lysates Lane 5: Human A431 cell lysates Primary: Anti-Tubulin-alpha (Loading Control) (bs-0159R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kDa Observed band size: 52 kDa
Sample: Lane 1: Mouse NIH/3T3 cell lysates Lane 2: Human HepG2 cell lysates Lane 3: Human 293T cell lysates Primary: Anti-Tubulin-alpha (Loading Control) (bs-0159R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kDa Observed band size: 52 kDa
Sample: MOLT-4(Human) Cell Lysate at 30 ug Primary: Anti-Tubulin-alpha (bs-0159R) at 1/2000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 50 kD
Sample: Heart (Mouse) Lysate at 40 ug Primary: Anti- Tubulin-alpha (bs-0159R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 52 kD
Sample: Lane 1: Cerebrum (Rat) Lysate at 40 ug Lane 2: Cerebrum (Mouse) Lysate at 40 ug Lane 3: Cerebellum (Rat) Lysate at 40 ug Lane 4: Cerebellum (Mouse) Lysate at 40 ug Primary: Anti-Tubulin-alpha (bs-0159R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 50 kD
Sample: Cerebrum (Mouse) Lysate at 40 ug Cerebellum (Mouse) Lysate at 40 ug Primary: Anti-Tubulin-alpha(bs-0159R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50kD Observed band size: 55kD
Sample: Hela(Human) Cell Lysate at 30 ug Primary: Anti-Tubulin-alpha (bs-0159R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 50 kD
Blank control: RSC96 Cells (blue). Primary Antibody:Rabbit Anti- Tubulin-alpha 1 antibody(bs-0159R), Dilution: 1μg in 100 μL 1X PBS containing 0.5% BSA; Isotype Control Antibody: Rabbit IgG(orange) ,used under the same conditions ); Secondary Antibody: Goat anti-rabbit IgG-PE(white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA. Protocol The cells were fixed with 2% paraformaldehyde (10 min) , then permeabilized with 90% ice-cold methanol for 30 min on ice. Primary antibody (bs-0159R,1μg /1x10^6 cells) were incubated for 30 min on the ice, followed by 1 X PBS containing 0.5% BSA + 1 0% goat serum (15 min) to block non-specific protein-protein interactions. Then the Goat Anti-rabbit IgG/PE antibody was added into the blocking buffer mentioned above to react with the primary antibody at 1/200 dilution for 30 min on ice. Acquisition of 20,000 events was performed.
 
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