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NIPT Reference Standard
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Package-Ref™ HRD Cocktail Reference Standard

Material Number: CBP90023
Size: 1ug
 

Package-Ref™ MRD Cocktail Reference Standard

Material Number: CBP90040
Size: 1ug
 

tTMB-P9(matrix) Reference Standard

Material Number: CBP80001-9
Size: 1ug
 

Panel-Ref® RNA-Fusion Cocktail Control

Material Number: CBP90001
Size: 1ug
 

Panel-Ref® HRR-Related-28 Gene Cocktail Reference Standard

Material Number: CBP90044
Size: 1ug
 

NIPT Plasma Reference Standard

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Material Number: CBPJ00019-CBPJ0023
Size: 1.2 mL
 

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PCR Development

ISA (integration site analysis)

Customized Materials

About Us

CB-Gene's Genetic Testing:

Turning the Mystery of Your DNA Into Clear, Actionable Health Advice.
Nanjing CB-Gene Biotechnology Co., Ltd. was established in 2020 and is located in Nanjing, China.We mainly provide highly characterized and precisely defined diagnostic reference materials and quality control materials to help you analyze the sensitivity, specificity and stability of experiments.
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Advanced Genetic Testing Meets Personalized 

Wellness, Illuminating Your Path To Well - Being.

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News

11/ 07/ 2025

Is It Better To Be HRD Positive or Negative?

You may hear your doctor say HRD positive or HRD negative when talking about cancer. HRD positive means your cells cannot fix DNA damage well. HRD negative means your cells fix DNA damage easily. About half of patients are in each group:Knowing your HRD status helps doctors choose your treatment.

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11/ 04/ 2025

What Is HRD Testing and How Does It Impact Cancer Diagnosis

You can use HRD testing to see if a tumor cannot fix DNA. This test helps doctors pick the best treatment for you. It is very useful for ovarian, breast, and prostate cancer. Many patients with non-BRCA1/2 gene changes show HRD positivity. Germline mutations often cause even higher rates.

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09/ 11/ 2024

BCR-ABL Fusion Diagnostic Reference Standard

​CB-Gene Bio can provide diagnostic standards for BCR-ABL1 fusion and fusion + mutation types to ensure the detection limit, sensitivity and stability of the diagnostic method.

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Lentivirus Integration Standard
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