目录产品 » Integrin alpha 2B beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse

Integrin alpha 2B beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse

Glanzmann thrombasthenia (GT) is characterized by mucocutaneous bleeding due to platelets that fail to aggregate in response to physiologic stimuli. GT, a rare inherited disease, is caused by quantitative or qualitative deficiencies of αIIbβ3, an integrin receptor for adhesive proteins. Coded by the ITGA2B and ITGB3 genes, αIIbβ3 mediates platelet-to-platelet attachment, aggregation and clot retraction.
¥4100
Z06222-100

Species Mouse
Protein Construction
Integrin alpha 2B beta 3 (ITGA2B&ITGB3) Heterodimer[Leu32-Arg988 (ITGA2B) acidic tail and Glu26-Asp717 (ITGB3) basic tail]
Accession # Q9QUM0(ITGA2B)&O54890(ITGB3)
His
N-term C-term
Purity > 95% as determined by Bis­Tris PAGE 
> 90% as determined by HPLC
Endotoxin Level Less than 1EU per μg by the LAL method.
Expression System HEK293
Theoretical Molecular Weight 109.80 kDa (ITGA2B) and 80.80 kDa (ITGB3)
Apparent Molecular Weight Due to glycosylation, the protein migrates to 90-113 kDa based on Bis-Tris PAGE result.
Formulation Lyophilized from 0.22μm filtered solution in PBS (pH 7.4).
Reconstitution Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/ml is recommended. Dissolve the lyophilized protein in distilled water.
Storage & Stability Upon receiving, the product remains stable up to 6 months at -20 °C or below. Upon reconstitution, the product should be stable for 3 months at -80 °C. Avoid repeated freeze-thaw cycles.
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Integrin Alpha 2B Beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse

The purity of Integrin alpha 2B beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse is greater than 90% as determined by SEC-HPLC. »

Integrin Alpha 2B Beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse

Integrin alpha 2B beta 3 (ITGA2B&ITGB3) Heterodimer, His, Mouse on Bis-Tris PAGE under reduced condition. The purity is greater than 95%. »

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Target Background Glanzmann thrombasthenia (GT) is characterized by mucocutaneous bleeding due to platelets that fail to aggregate in response to physiologic stimuli. GT, a rare inherited disease, is caused by quantitative or qualitative deficiencies of αIIbβ3, an integrin receptor for adhesive proteins. Coded by the ITGA2B and ITGB3 genes, αIIbβ3 mediates platelet-to-platelet attachment, aggregation and clot retraction.
Synonyms α2Bβ3; ITGA2B&ITGB3; ITGA2B; ITGB3
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For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.