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SMAL1 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN3272
产品名称
SMAL1 Rabbit Polyclonal Antibody
别名
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1 (EC 3.6.4.-) (HepA-related protein) (hHARP) (Sucrose nonfermenting protein 2-like 1)
类别
常规抗体
基因名称
SMARCAL1 HARP
蛋白名称
SMAL1
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.230% New type preservative N.
Human Gene ID
50485
Human Gene Link
https://www.uniprot.org/uniprot/50485
Human Swissprot No.
Q9NZC9
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q9NZC9/entry
Mouse Gene ID
54380
Mouse Gene Link
https://www.uniprot.org/uniprot/54380
Mouse Swissprot No.
Q8BJL0
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q8BJL0
Rat Gene ID
316477
Rat Gene Link
https://www.uniprot.org/uniprot/316477
Rat Swissprot No.
B4F769
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/B4F769
免疫原
Synthesized peptide derived from human SMAL1 AA range: 485-535
特异性
This antibody detects endogenous levels of SMAL1 at Human/Mouse/Rat
稀释度
WB 1:500-2000
预测分子量
105kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008],
组织表达
Ubiquitously expressed, with high levels in testis.
细胞定位
Nucleus . Recruited to damaged DNA regions.
功能
disease:Defects in SMARCAL1 are a cause of Schimke immuno-osseous dysplasia (SIOD) [MIM:242900]. SIOD causes spondyloepiphyseal dysplasia, renal dysfunction and T-cell immunodeficiency. Approximately half of all patients also exhibit hyperthyroidism, while around half also exhibit episodal cerebral ischema.,function:ATP-dependent annealing helicase that catalyzes the rewinding of the stably unwound DNA. Rewinds single-stranded DNA bubbles that are stably bound by replication protein A (RPA). Acts throughout the genome to reanneal stably unwound DNA, performing the opposite reaction of many enzymes, such as helicases and polymerases, that unwind DNA.,online information:SMARCAL1 mutation db,similarity:Belongs to the SNF2/RAD54 helicase family. SMARCAL1 subfamily.,similarity:Contains 1 helicase ATP-binding domain.,similarity:Contains 1 helicase C-terminal domain.,similarity:Contains 2 HARP domains.,tissue specificity:Ubiquitously expressed, with high levels in testis.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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