ATRX-Specific抗体-抗体-抗体-生物在线
上海信裕生物科技有限公司
ATRX-Specific抗体

ATRX-Specific抗体

商家询价

产品名称: ATRX-Specific抗体

英文名称: ATRX-SpecificAntibody

产品编号: XY19788-1

产品价格: null

产品产地: 中国/美国

品牌商标: XYbscience

更新时间: 2023-08-17T09:55:27

使用范围: WB,ELISA,IHC-P,IHC-F,IF

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 ATRX-SPECIFIC抗体

Applications
Tested Applications: ELISA
Specificity Reaction: Human; Other species are not tested.Please decide the specificity by homology
Recommended dilution  
 ATRX-SPECIFIC抗体Application key: WB=Western Blotting ,IHC=Immunohistochemistry, IF=Immunofluorescence
Product Information
Source: Rabbit Purify: Antigen affinity purification
IsoType: IgG Storage: PBS with 0.1% sodium azide and 50% glycerol pH 7.3. -20oC, Avoid freeze / thaw cycles.
Immunogen Information
Immunogen: Peptide Full Name: Alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
Caculated Molecular
Weight:
283 kDa Observed Molecular 
Weight:
 
GenbankNo NM_000489 GeneID: 546
Symbol ATRX Synonyms ATP dependent helicase ATRX, ATR2, ATRX, MRXHF1, RAD54, RAD54L, SFM1, SHS, Transcriptional regulator ATRX, X linked helicase II, X linked nuclear protein, XH2, XNP, ZNF HX
Background ATRX-SPECIFIC抗体

ATRX, also named as RAD54L and XH2, belongs to the SNF2/RAD54 helicase family. ATR could be a global transcriptional regulator. ATRX modifies gene expression by affecting chromatin. It may be involved in brain development and facial morphogenesis. Defects in ATRX are the cause of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X) which is an X-linked disorder comprising severe psychomotor retardation, facial dysmorphism, urogenital abnormalities, and alpha-thalassemia. Defects in ATRX are the cause of mental retardation syndromic X-linked with hypotonic facies syndrome type 1 (MRXSHF1) which also called Carpenter-Waziri syndrome (CWS), Juberg-Marsidi syndrome (JMS), Smith-Fineman-Myers syndrome type 1 (SFM1). This antibody is specific to ATRX. ATRX-SPECIFIC抗体

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