18P-syndrome (46,XX,del(18)(p11.2)) Reference Standard

CBPJ0008

詢(xún) 價(jià)

索取COA

產(chǎn)品描述

產(chǎn)品數據庫

Introduction　

Name

18P-syndrome (46,XX,del(18)(p11.2)) Reference Standard

Format

Genomic DNA

Technical Data　

Mutation

18P-syndrome

Karyotype

46,XX,del(18)(p11.2)

Representative Data

Z-Score：

chr

chrl

chr2

chr3

chr4

chr5

chr6

chr7

chr8

chr9

chr10

chrll

chr12

chrl3

chr14

chr15

chr16

chr17

chr18

chr19

chr20

chr21

chr22

CBPJ0008

3.16

-1.79

2.00

0.84

-0.02

2.26

2.46

-1.75

-0.62

-2.27

1.26

3.04

0.68

1.61

-0.15

-1.33

1.57

-21.78

2.94

-1.30

0.09

-1.41

Product Information　

Intended Use

Research Use Only

Unit Size

1ug

Concentration

Download for COA

DNA electrophoresis

Download for COA

Storage

4°C

Expiry

36 months from the date of manufacture

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上一篇：Prader-Willi syndrome (46,XY,del(15)(q11.2q13)) Reference Standard

下一篇：Trisomy 21 (47,XY,+21) Reference Standard

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藥靶模型聯(lián)系方式: 華東銷(xiāo)售經(jīng)理：18240630236 全國銷(xiāo)售經(jīng)理：18066071954
診斷標準品聯(lián)系方式：華東銷(xiāo)售經(jīng)理：15000320447 華北銷(xiāo)售經(jīng)理：18131625521 華南銷(xiāo)售經(jīng)理：13484295986 華中&西南銷(xiāo)售經(jīng)理：13871580511 全國銷(xiāo)售經(jīng)理：13484295986

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18P-syndrome (46,XX,del(18)(p11.2)) Reference Standard