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SOX9 抗体
SOX9
适用: 人
WB, IHC, IF, IP
宿主: 兔
Monoclonal
unconjugated
SOX9抗体详情
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抗原
See all SOX9 抗体
SOX9
(SRY (Sex Determining Region Y)-Box 9 (SOX9))
适用
All reactivities for SOX9 抗体
人
宿主
All hosts for SOX9 抗体
兔
克隆类型
All clonalities for SOX9 抗体
单克隆
标记
All conjugates for SOX9 抗体
This SOX9 antibody is un-conjugated
应用范围
All applications for SOX9 抗体
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
原理
SOX9 Rabbit mAb
交叉反应
人, 小鼠, 大鼠
产品特性
Monoclonal Antibodies
纯化方法
Affinity purification
免疫原
A synthesized peptide derived from human SOX9.
亚型
IgG
Top Product
Discover our top product SOX9 Primary Antibody
Alternatives
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anti-SRY (Sex Determining Region Y)-Box 9 (SOX9) (C-Term) antibody
SOX9
适用: 人, 小鼠, 大鼠, 兔, 犬, Pig, 斑马鱼, Cow, 豚鼠, 马
WB, FACS
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200,IP,1:50 - 1:200
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
SOX9目标详情
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抗原
SOX9
(SRY (Sex Determining Region Y)-Box 9 (SOX9))
别名
SOX9 (SOX9 产品 )
别名
CMD1 antibody, CMPD1 antibody, SRA1 antibody, LOC100227849 antibody, 2010306G03Rik antibody, AV220920 antibody, mKIAA4243 antibody, SOX-9 antibody, cmd1 antibody, cmpd1 antibody, sox-9 antibody, sox9 antibody, sox9-a antibody, sox9-b antibody, sox9b antibody, sra1 antibody, SRY-box 9 antibody, transcription factor SOX-9 antibody, SRY (sex determining region Y)-box 9 antibody, SRY box 9 antibody, SRY-box 9 L homeolog antibody, SOX9 antibody, LOC100227849 antibody, Sox9 antibody, sox9.L antibody
背景
The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008],CMD1,CMPD1,SRA1,SRXX2,SRXY10,SOX9,SRY-box 9,Apoptosis,Cell Biology & Developmental Biology,Epigenetics & Nuclear Signaling,Mesenchymal Stem Cells,Neural Stem Cells,Neuroscience,Stem Cells,Transcription Factors,SOX9
分子量
70kDa
基因ID
6662
UniProt
P48436
途径
EGFR Signaling Pathway , Stem Cell Maintenance , Regulation of Muscle Cell Differentiation , Tube Formation , Skeletal Muscle Fiber Development
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