Recombinant Rat Erbb2, Fc tagged

• Cat.No.: Erbb2-4097R
• Product Overview: Recombinant Rat Erbb2 (AAH61863.1) extracellular domain (Met 4-Thr 656), fused with the Fc region of human IgG1 at the C-terminus, was produced in Human Cell.

Specification

• Species: Rat
• Source: Human Cells
• Tag: Fc
• Protein Length: 4-656 a.a.
• Form: Lyophilized from sterile PBS, pH 7.4
• Molecular Mass: The recombinant rat ErbB2/Fc is a disulfide-linked homodimer. The reduced monomer comprises 872 amino acids and predicts a molecular mass of 97 kDa. The apparent molecular mass of the rat ErbB2/Fc monomer is approximately 130 kDa in SDS-PAGE under reducing conditions due to glycosylation.
• Endotoxin: < 1.0 eu per μg of the protein as determined by the LAL method.
• Stability: Samples are stable for up to twelve months from date of receipt at -70oC.
• Storage: Store it under sterile conditions at -20oC~-70oC. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
• Reconstitution: It is recommended that sterile water be added to the vial to prepare a stock solution. Centrifuge the vial at 4℃ before opening to recover the entire contents.

Gene Information

• Gene Name: Erbb2 v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian) [ Rattus norvegicus ]
• Official Symbol: Erbb2
• Gene ID: 24337
• mRNA Refseq: NM_017003
• Protein Refseq: NP_058699

Q&As

Do you have a recommended protocol for immobilizing any avi-tagged recombinant proteins on a streptavidin coated plate?

1.Prepare the streptavidin-coated plate by washing it with PBS (phosphate-buffered saline) or another suitable buffer to remove any impurities. 2.Dilute the Avi-tagged protein in the desired buffer at the desired concentration. It is important to use a buffer that is compatible with the protein and does not interfere with its activity or stability. 3.Add the diluted protein to the streptavidin-coated plate and incubate it for a suitable amount of time at room temperature or 4°C. The exact conditions will depend on the specific protein and the desired level of immobilization. 4.Wash the plate with a suitable buffer to remove any unbound protein. 5.Block the remaining binding sites on the plate with a suitable blocking agent such as BSA (bovine serum albumin) or casein. 6.Wash the plate again to remove any unbound blocking agent. 7.Use the immobilized protein for further experiments such as ELISA, Western blotting, or other assays.