13916964679
Note: Application as IHC, only suitable for histochemical staining or fluorescence staining of paraffin-embedded sections. Application as ICC/IF, suitable for histochemical or fluorescent staining of frozen sections, as well as chemical and fluorescent staining at the cellular level.
注意：抗体应用为IHC的，抗体只适合于石蜡切片的组化染色或者荧光染色。
抗体应用为IF/ICC的，抗体适合于冰冻切片的组化染色或者荧光染色，以及细胞水平的化学染色和荧光染色。
ABMART实验方案下载
This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
FLJ10267;
MGC986;
NOL1;
NOL1-related protein;
NOL1/NOP2/Sun domain family member 5;
NOL1R;
NOP2/Sun domain family, member 5;
NOP2/Sun domain family, member 5A;
NSUN5;
NSUN5_HUMAN;
p120;
Putative methyltransferase NSUN5;
WBSCR20;
WBSCR20A;
Williams Beuren syndrome chromosome region 20A;
Williams-Beuren syndrome chromosomal region 20A protein;
Williams-Beuren syndrome critical region protein 20 copy A.
Human
WB
WB 1:500-2000
47kD
55695
Q96P11
Ubiquitous. Detected in placenta, heart and skeletal muscle.
KLH conjugated synthetic peptide derived from human NSUN5
Rabbit
Polyclonal
IgG
affinity purified by Protein A
Liquid
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
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应聘职位：hr@ab-mart.com
订购专线：4006-123-828
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程经理：手机18616261485（微信同号）
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徐经理：手机15618191473（微信同号）
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陆经理：手机13122837132（微信同号）
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