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抑癌基因SNF2β抗體
  • 產品貨號：
    BN41706R
  • 中文名稱：
    抑癌基因SNF2β抗體
  • 英文名稱：
    Rabbit anti-BRG-1 Polyclonal antibody
  • 品牌：
    Biorigin

  • 貨號

    產品規(guī)格

    售價

    備注

  • BN41706R-50ul

    50ul

    ￥1486.00

    交叉反應：Human,Rat(predicted:Mouse,Dog) 推薦應用：IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41706R-100ul

    100ul

    ￥2360.00

    交叉反應：Human,Rat(predicted:Mouse,Dog) 推薦應用：IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41706R-200ul

    200ul

    ￥3490.00

    交叉反應：Human,Rat(predicted:Mouse,Dog) 推薦應用：IHC-P,IHC-F,IF,Flow-Cyt,ELISA

產品描述

英文名稱BRG-1
中文名稱抑癌基因SNF2β抗體
別    名BRG1; ATP dependent helicase SMARCA4; BAF 190; BAF190; BAF190A; Brahma protein homolog 1; Brahma protein like 1; BRG 1; BRG 1 protein; BRG1; BRG1 associated factor 190A; BRG1 protein; BRM/SWI2 related gene 1; Global transcription activator homologous sequence; Homeotic gene regulator; hSNF2b; Mitotic growth and transcription activator; Nuclear protein GRB1; Probable global transcription activator SNF2L4; Protein brahma homolog 1; Protein BRG1; SMARC A4; SMARCA 4; SMARCA4; SNF 2; SNF 2B; SNF2;;brahma-related gene 1; SNF2 beta; SNF2 like 4; SNF2B; SNF2beta; SNF2L4; SNF2LB; SWI 2; SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily A member 4; SWI2; Transcription activator BRG1.  






研究領域腫瘤  免疫學  細胞凋亡  轉錄調節(jié)因子  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應Human, Rat,  (predicted: Mouse, Dog, )
產品應用ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=3ug/test IF=1:100-500 （石蠟切片需做抗原修復）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量185kDa
細胞定位細胞核 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human SMARCA4:51-167/1647 
亞    型IgG
純化方法affinity purified by Protein A
儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產品介紹The protein encoded by this gene is a member of the SWI/SNF family of proteins and is similar to the brahma protein of Drosophila. 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 is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. In addition, this protein can bind BRCA1, as well as regulate the expression of the tumorigenic protein CD44. Alternatively spliced transcripts have been found for this gene, but their full-length natures have not been determined.

Function:
Transcriptional coactivator cooperating with nuclear hormone receptors to potentiate transcriptional activation. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a post-mitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state.

Subunit:
Belongs to the SNF2/RAD54 helicase family. Contains 1 bromo domain. Contains 1 helicase ATP-binding domain. Contains 1 helicase C-terminal domain. Contains 1 HSA domain.

Tissue Specificity:
Colocalizes with ZEB1 in E-cadherin-negative cells from established lines, and stroma of normal colon as well as in de-differentiated epithelial cells at the invasion front of colorectal carcinomas (at protein level).

DISEASE:
Defects in SMARCA4 are the cause of rhabdoid tumor predisposition syndrome type 2 (RTPS2). RTPS2 is a familial cancer syndrome predisposing to renal or extrarenal malignant rhabdoid tumors and to a variety of tumors of the central nervous system, including choroid plexus carcinoma, medulloblastoma, and central primitive neuroectodermal tumors. Rhabdoid tumors are the most aggressive and lethal malignancies occurring in early childhood.

SWISS:
P51532

Gene ID:
6597

Database links:

Entrez Gene: 6597 Human

Entrez Gene: 20586 Mouse

Entrez Gene: 171379 Rat

Omim: 603254 Human

SwissProt: P51532 Human

SwissProt: Q3TKT4 Mouse

SwissProt: Q8K1P7 Rat

Unigene: 327527 Human

Unigene: 286593 Mouse

Unigene: 23417 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

轉錄調節(jié)因子（Transcriptin Regulators）
SMARCA4是一種新的抑癌基因，已在許多腫瘤的研究中發(fā)現它是一種重要的抑癌基因，很多腫瘤的發(fā)生與其功能失活或出現基因突變、缺失相關聯。