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`Application No. 15/121,623
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`- 7 -
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`GEUIJEN er a].
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`AATAATTCTAGACTGGCACGTCCAGACCCAGG
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`AAGCTGGCTAGCACCATGGAGCTGGCGGCCTTGTGC gSEQ ID NO: 41 The full-length
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`amplified product was digested with NheI-XbaI and subsequently cloned in the corresponding sites
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`of pcDNA3.1. The clone was sequenced and aligned with sequences available of rhesus monkeys
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`()flVI_OO280045 1) to check correctness of the ErbB-2 clone.
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`Cynomolgus HER3 extracellular domain was PCR amplified from cynomolgus cDNA--Monkey)
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`Normal Colon Tissue (Biochain). The primers used for the amplification of cynomolgus HER3
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`were as follows:
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`Forward primer: AAGCTGGCTAGCACCATGAGGGCGAACGGCGCTCTG
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`AAGCTGGCTAGCACCATGGAGCTGGCGGCCTTGTGC gSEgg ID NO: 51, Reversed primer:
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`AATAATTCTAGATTACGTTCTCTGGGCATTAGC
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`AAGCTGGCTAGCACCATGGAGCTGGCGGCCTTGTGC gSEQ ID NO: 61The full-length
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`amplified product was digested with NheI-XbaI and subsequently cloned in the corresponding sites
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`of pcDNA3.1. The clone was sequenced and aligned with sequences available of rhesus monkeys
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`(ENSMMUPOOOOOO27321) to check correctness of the HER3 clone.
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`Please amend the paragraph beginning on page 95, line 13 as follows:
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`The monovalent binding affinity of PB4188 and PB3448 for recombinant HER2 and HER3 was
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`determined by SPR (Biacore T100). BIACOREBiaeereTM. ..
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`Atty. Dkt. No. 4096.0100002/DAS/PAC/E-H
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