TUBA1A Monoclonal Antibody | CSB-MA754656A0m

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SKU:
CSB-MA754656A0m
Availability:
3 to 7 Working Days
  • TUBA1A Monoclonal Antibody
  • Western Blot<br />
 Positive WB detected in: U87 whole cell lysate, PC-3 whole cell lysate, 293 whole cell lysate, U251 whole cell lysate, A549 whole cell lysate, A375 whole cell lysate, MG-63 whole cell lysate, SH-SY5Y whole cell lysate, <br />
 All lanes: TUBA1A antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Rabbit heatrt tissue, Rabbit liver tissue, Rabbit spleen tissue, Rabbit lung tissue, Rabbit kidney tissue, Rabbit small intestine tissue, Rabbit skeletal muscle tissue<br />
 All lanes: TUBA1A antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Rat brain tissue, Rat stomach tissue, Rat kidney tissue<br />
 All lanes: TUBA1A antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: NIH/3T3 whole cell lysate, RAW264.7 whole cell lysate, Mouse brain tissue, Mouse kidney tissue<br />
 All lanes: TUBA1A antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Hela whole cell lysate at 20µg, 10µg, 5µg, 2.5µg, 1.25µg<br />
 All lanes: TUBA1A antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Hela whole cell lysate<br />
 All lanes: TUBA1A antibody at 1:2500, 1:5000, 1:10000, 1:20000, 1:40000, 1:80000, 1:160000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Hela whole cell lysate at 20µg, 10µg, 5µg, 2.5µg, 1.25µg, 0.625µg, 0.3125µg, 0.15625µg<br />
 All lanes: Company A, Company B, Company C, Company D, CSB-MA754656A0m antibody at 1:5000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • Western Blot<br />
 Positive WB detected in: Hela whole cell lysate<br />
 All lanes: Company A, Company B, Company C, Company D, CSB-MA754656A0m antibody at 1:2500, 1:5000, 1:10000, 1:20000, 1:40000, 1:80000, 1:160000, 320000<br />
 Secondary<br />
 Goat polyclonal to Mouse IgG at 1/10000 dilution<br />
 Predicted band size: 52 kDa<br />
 Observed band size: 52 kDa<br />
  • IHC image of CSB-MA754656A0m diluted at 1:150 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
  • IHC image of CSB-MA754656A0m diluted at 1:150 and staining in paraffin-embedded human breast cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
  • Immunofluorescence staining of Hela cells with CSB-MA754656A0m at 1:75, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
  • Immunoprecipitating TUBA1A in Hela whole cell lysate<br />
 Lane 1: Mouse control IgG (1µg) instead of CSB-MA754656A0m in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)<br />
 Lane 2: CSB-MA754656A0m (5µg) + Hela whole cell lysate (500µg)<br />
 Lane 3: Hela whole cell lysate (20µg)<br />
  • Immunoprecipitating TUBA1A in Hela whole cell lysate<br />
 Lane 1: Mouse control IgG (1µg) instead of CSB-MA754656A0m in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)<br />
 Lane 2: Company A (5µg), Company B (5µg), Company C (5µg), Company D (5µg), CSB-MA754656A0m (5µg) + Hela whole cell lysate (500µg)<br />
 Lane 3: Hela whole cell lysate (20µg)<br />
  • Overlay histogram showing Hela cells stained with CSB-MA754656A0m (red line) at 1:150. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
  • Overlay histogram showing Hela cells stained with Company A (5µg), Company B (5µg), Company C (5µg), Company D (5µg), CSB-MA754656A0m (5µg) (red line) at 1:150. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
  • Overlay histogram showing Hela cells stained with CSB-MA754656A0m (red line) at 1:150. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
  • Overlay histogram showing Hela cells stained with Company A (5µg), Company B (5µg), Company C (5µg), Company D (5µg), CSB-MA754656A0m (5µg) (red line) at 1:150. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
€256.00 - €360.00
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Description

TUBA1A Monoclonal Antibody | CSB-MA754656A0m | Cusabio

TUBA1A Monoclonal Antibody is Available at Gentaur Genprice with the fastest delivery.

Online Order Payment is possible or send quotation to info@gentaur.com.

Product Type: Tag/Control Antibodies

Target Name: TUBA1A

Aliases: Tubulin alpha-1A chain

Relevance: Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain.

Isotype: IgG2b

Conjugate: Non-conjugated

Clone Number: 7E5C12

Host Species: Mouse

Species Reactivity: Human, Rabbit, Rat, Mouse

Immunogen: A synthesized peptide derived from human Tubulin alpha-1A chain (297-309)

Applications: ELISA, WB, IHC, IF, FC, IP

Tested Applications: ELISA, WB, IHC, IF, FC, IP; Recommended dilution: WB: 1:20000-1:320000, IHC: 1:100-1:300, IF: 1:50-1:200, FC: 1:100-1:300, IP: 1µg-5µg

Purification Method: >95%,Protein A purified

Dilution Ratio1: WB:1:20000-1:320000

Dilution Ratio2: IHC:1:100-1:300

Dilution Ratio3: IF:1:50-1:200

Dilution Ratio4: FC:1:100-1:300

Dilution Ratio5: IP:1µg-5µg

Buffer: Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4

Form: Liquid

Storage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

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