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科研原料 SOX9 (ABT-SOX9) Mouse mAb

说明书

BYab-34720

  • 20uL ¥680 50uL ¥1340 100uL ¥1800
  • 货期: 3个工作日

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宿主
反应性
应用
WB、IHC、IF、ELISA
分子量(DA)
免疫原
Synthesized peptide derived from human SOX9 AA range: 1-100
特异性
The antibody can specifically recognize human SOX9 protein. In western blotting of SW480 and HepG2 cell lysates, the antibody can label a 60 kDa band corresponding to SOX9.
来源
组成(Formulation)
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
稀释比例
IHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000 Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#YS0004)
纯化工艺(Immunogen)
Recombinant Antibody expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography.
浓度
1 mg/ml
背景(Background)
Sox9 is a transcription factor that plays a key role in chondrocyte differentiation and bone development. It is expressed in cartilage , neural crest , kidney and pancreas.
功能
Disease:Defects in SOX9 are the cause of campomelic dysplasia (CMD1) [MIM:114290]. CMD1 is a rare , often lethal , dominantly inherited , congenital osteochondrodysplasia , associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones , unusually small scapulae , deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate , micrognatia , flat face and hypertelorism are common. Various defects of the ear are often evident , affecting the cochlea , malleus incus , stapes and tympanum. Most patients die soon after birth due to respiratory distress which has been attributed to hypoplasia of the tracheobronchial cartilage and small thoracic cage. ,Function:Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. ,similarity:Contains 1 HMG box DNA-binding domain. ,
基因名称(Gene Name)
SOX9
蛋白名称
Transcription factor SOX-9
简称
campomelic dysplasia autosomal sex reversal ; CMD 1 ; CMD1 ; CMPD 1 ; CMPD1 ; SOX 9 ; Sox9 ; SOX9_HUMAN ; SRA 1 ; SRA1 ; SRXX2 ; SRXY10 ; SRY ; sex determining region Y ; box 9 ; campomelic dysplasia autosomal ; SRY ; sex determining region Y ; box 9 ; SRY ; sex determining region Y ; -box 9 ; SRY ; sex-determining region Y ; -box 9 protein ; SRY related HMG box gene 9 ; Transcription factor SOX 9 ; Transcription factor SOX-9 ; transcription factor SOX9
其他名称
=_xlfn.TEXTJOIN(";",TRUE,W3195,X3195,Y3195,Z3195)
Fields
人基因ID
6662
人蛋白质序列数据库
P48436
小鼠基因ID
20682
小鼠蛋白质序列数据库
Q04887
大鼠基因ID
大鼠蛋白质序列数据库
细胞定位
Nuclear
组织表达
Eye ,PNS ,Testis ,
储存(Storage)
-15°C to -25°C/1 year(Do not lower than -25°C)

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科研原料 SOX9 (ABT-SOX9) Mouse mAb

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