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Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.

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Hybribio Thalassemia GenoArray Diagnostic Kits
Hybribio Thalassemia GenoArray Diagnostic Kits

β-,thalassemia, is due to the deficiency of β globin chains encoded by a single ,gene, on chromosome 11. Hybribio ,Thalassemia Gene, Diagnostic ,Kit, provides an ‘All-In-One’ platform for screening of BOTH alpha and beta ,thalassemia, with detailed information of diagnosis in terms of heterozygosity and homozygosity for all positive results.

Thalassemia Gene Diagnostic Kit | Guangzhou Hybribio ...
Thalassemia Gene Diagnostic Kit | Guangzhou Hybribio ...

β-,thalassemia, is due to the deficiency of β globin chains encoded by a single ,gene, on chromosome 11. Hybribio ,Thalassemia Gene, Diagnostic ,Kit, provides an ‘All-In-One’ platform for screening of BOTH alpha and beta ,thalassemia, with detailed information of diagnosis in terms of heterozygosity and homozygosity for all positive results.

Thalassemia Gene Diagnostic Kit | Guangzhou Hybribio ...
Thalassemia Gene Diagnostic Kit | Guangzhou Hybribio ...

β-,thalassemia, is due to the deficiency of β globin chains encoded by a single ,gene, on chromosome 11. Hybribio ,Thalassemia Gene, Diagnostic ,Kit, provides an ‘All-In-One’ platform for screening of BOTH alpha and beta ,thalassemia, with detailed information of diagnosis in terms of heterozygosity and homozygosity for all positive results.

KRAS Mutation Detection Kit | LCM Genect Detection kit
KRAS Mutation Detection Kit | LCM Genect Detection kit

Il KRAS Mutation ,Detection Kit, permette il rilevamento delle mutazioni sui codoni 12, 13, 59, 61, 117 e 146 del ,gene, KRAS in un test PCR in tempo reale

Genetic Testing for Beta Thalassemia | Mapmygenome
Genetic Testing for Beta Thalassemia | Mapmygenome

We offer the following tests: Beta ,Thalassemia, Mutation Analysis: This test analyses DNA (extracted from whole blood) for the major mutations found in the HBB ,gene, which represent the mutation spectrum found in Indian thalassemic subjects-(IVS 1-5 G>C, IVS 1-1 G>T, 619 bp deletion, Codon 15 G>A, Codon 30 G>A, FS 8/9 +G, FS 41/42 – CTTT). Molecular analysis is done via PCR (amplification of ...

Molecular testing techniques for Thalassemia?
Molecular testing techniques for Thalassemia?

I need to know which is the best technique to diagnose ,Thalassemia, (Alpa and Beta). I would like to use a molecular test (RT- or conventional PCR, Sequencing...) and which ,kit, are should be used.

AccuPid Beta- Thalassemia Genotyping Kit - kt-biotech
AccuPid Beta- Thalassemia Genotyping Kit - kt-biotech

AccuPid Beta-,Thalassemia Kit, là công cụ hữu ích cho công tác nghiên cứu, chẩn đoán 8 đột biến gây bệnh beta-,thalassemia, thường gặp nhất trong quần thể người Việt Nam và phát hiện bệnh β- ,Thalassemia,/HbE. 8 vị trí đột biến xuất hiện trên gen hbb: -28(A → G); codon 17 (A → T); codon 26 […]

Genetic Testing for Beta Thalassemia | Mapmygenome
Genetic Testing for Beta Thalassemia | Mapmygenome

We offer the following tests: Beta ,Thalassemia, Mutation Analysis: This test analyses DNA (extracted from whole blood) for the major mutations found in the HBB ,gene, which represent the mutation spectrum found in Indian thalassemic subjects-(IVS 1-5 G>C, IVS 1-1 G>T, 619 bp deletion, Codon 15 G>A, Codon 30 G>A, FS 8/9 +G, FS 41/42 – CTTT). Molecular analysis is done via PCR (amplification of ...

Laboratory diagnosis of thalassemia - Brancaleoni - 2016 ...
Laboratory diagnosis of thalassemia - Brancaleoni - 2016 ...

Xiaozhe Lin, Bizhen Cheng, Yingmu Cai, Xiaoyang Jiao, Xinran Yang, Qiaoxin Zhang, Yongni Wang, Establishing and evaluating an auto-verification system of ,thalassemia gene detection, results, Annals of Hematology, 10.1007/s00277-019-03656-4, (2019).

Thalassemia | Genetic and Rare Diseases Information Center ...
Thalassemia | Genetic and Rare Diseases Information Center ...

1/1/2015, · There are two main types of ,thalassemia,, alpha ,thalassemia, and beta ,thalassemia,, which each affect a different part of hemoglobin (the protein in red blood cells that carries oxygen). Hemoglobin is made up of two different components (subunits): beta globin and alpha globin. The HBB ,gene, provides instructions for making beta globin, while the HBA1 and HBA2 ,genes, provide instructions for making ...

Beta Thalassemia - Xcelris Medical Genetics
Beta Thalassemia - Xcelris Medical Genetics

Mutation ,Detection, Test Beta ,Thalassemia, Mutation ,Thalassemia, is a hereditary genetic disorder in which the body makes an abnormal form of hemoglobin, a protein in red blood cells that carries oxygen. ,Thalassemia, occurs when our body is not able to produce sufficient amount of hemoglobin. It is caused by mutations in ,gene, encoding Beta globin ...

Evaluation of the BeTha Gene 1 Kit for the Qualitative ...
Evaluation of the BeTha Gene 1 Kit for the Qualitative ...

5National Center of ,Thalassemia,, Laikon General Hospital, Athens, Greece We describe the evaluation of the Bio-Rad BeTha ,Gene, 1 ,kit, (Bio-Rad Laboratories, Hercules, CA), a DNA-probe assay designed for the qualitative determination of the eight most common Mediteranean b-,thalassemia, mutations. The ,kit, utilizes the principle of

Laboratory diagnosis of thalassemia - Brancaleoni - 2016 ...
Laboratory diagnosis of thalassemia - Brancaleoni - 2016 ...

Xiaozhe Lin, Bizhen Cheng, Yingmu Cai, Xiaoyang Jiao, Xinran Yang, Qiaoxin Zhang, Yongni Wang, Establishing and evaluating an auto-verification system of ,thalassemia gene detection, results, Annals of Hematology, 10.1007/s00277-019-03656-4, (2019).

Genetic Testing for Beta Thalassemia | Mapmygenome
Genetic Testing for Beta Thalassemia | Mapmygenome

We offer the following tests: Beta ,Thalassemia, Mutation Analysis: This test analyses DNA (extracted from whole blood) for the major mutations found in the HBB ,gene, which represent the mutation spectrum found in Indian thalassemic subjects-(IVS 1-5 G>C, IVS 1-1 G>T, 619 bp deletion, Codon 15 G>A, Codon 30 G>A, FS 8/9 +G, FS 41/42 – CTTT). Molecular analysis is done via PCR (amplification of ...

AccuPid Beta- Thalassemia Genotyping Kit - kt-biotech
AccuPid Beta- Thalassemia Genotyping Kit - kt-biotech

AccuPid Beta-,Thalassemia Kit, là công cụ hữu ích cho công tác nghiên cứu, chẩn đoán 8 đột biến gây bệnh beta-,thalassemia, thường gặp nhất trong quần thể người Việt Nam và phát hiện bệnh β- ,Thalassemia,/HbE. 8 vị trí đột biến xuất hiện trên gen hbb: -28(A → G); codon 17 (A → T); codon 26 […]

Thalassemia Genotyping Kit ( PCR-Reverse Dot Blot ) – DOIT ...
Thalassemia Genotyping Kit ( PCR-Reverse Dot Blot ) – DOIT ...

This ,kit, is used for the in vitro qualitative ,detection, of human whole blood genomic DNA sample, which can detect the commonly seen 3 kinds of deletion type α-,thalassemia gene, mutation (–SEA, -α3.7 and -α4.2), 3 kinds of non-deletion type α-,thalassemia gene, mutation (αCSα, αQSα and αWSα) and 17 kinds of β-,thalassemia gene, mutation (41-42M, 654M, -28M, 71-72M, 17M, βEM, IVS-I-1M ...

Using PCR to Identify the Mutation of α-Thalassemia
Using PCR to Identify the Mutation of α-Thalassemia

The α-,thalassemia, involve the ,genes, HBA1 (Online Mendelian Inheritance in Man, OMIM, 141800) and HBA2 (Online Mendelian Inheritance in Man, OMIM, 141850). In this paper, the identification of mutation in HBA1 and HBA2 ,genes, which lead to α-,thalassemia, was analyzed by PCR and using specific primers to these two ,genes,.

Thalassemia Genotyping Kit ( PCR-Reverse Dot Blot ) – DOIT ...
Thalassemia Genotyping Kit ( PCR-Reverse Dot Blot ) – DOIT ...

This ,kit, is used for the in vitro qualitative ,detection, of human whole blood genomic DNA sample, which can detect the commonly seen 3 kinds of deletion type α-,thalassemia gene, mutation (–SEA, -α3.7 and -α4.2), 3 kinds of non-deletion type α-,thalassemia gene, mutation (αCSα, αQSα and αWSα) and 17 kinds of β-,thalassemia gene, mutation (41-42M, 654M, -28M, 71-72M, 17M, βEM, IVS-I-1M ...

Beta Thalassemia - Xcelris Medical Genetics
Beta Thalassemia - Xcelris Medical Genetics

Mutation ,Detection, Test Beta ,Thalassemia, Mutation ,Thalassemia, is a hereditary genetic disorder in which the body makes an abnormal form of hemoglobin, a protein in red blood cells that carries oxygen. ,Thalassemia, occurs when our body is not able to produce sufficient amount of hemoglobin. It is caused by mutations in ,gene, encoding Beta globin ...

Hybribio Thalassemia GenoArray Diagnostic Kits
Hybribio Thalassemia GenoArray Diagnostic Kits

β-,thalassemia, is due to the deficiency of β globin chains encoded by a single ,gene, on chromosome 11. Hybribio ,Thalassemia Gene, Diagnostic ,Kit, provides an ‘All-In-One’ platform for screening of BOTH alpha and beta ,thalassemia, with detailed information of diagnosis in terms of heterozygosity and homozygosity for all positive results.