LEF-1兔单克隆抗体

LEF-1兔单克隆抗体

  • 价格¥4688
  • 规格1ml
  • 货号HKI0961A
  • 单位
  • 品牌HaoKebio

产品介绍
产品参数
资料下载

2021/11/12一抗 910

品牌商品编码商品名称规格单位单价
HaoKebioHKI0961ALEF-1兔单克隆抗体100ul4688

Applications

Tested Applications:

IP, WB,ELISA


Cited Applications:

IF, IHC, WB


Species Specificity:

human, mouse, rat


Cited Species:

human, mouse


Positive WB detected in:

NCCIT cell, COLO 320 cells, Jurkat cells, SW 1990 cells


Positive IP detected in:

SW 1990 cells


Recommended dilution:

WB : 1:500-1:1000

IP : 0.5-4.0 ug for IP and 1:200-1:1000 for WB

Product Information


Source:

Rabbit


Purification method:

Antigen affinity purification


Isotype:

IgG


Storage:

PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Immunogen Information


Full name:

lymphoid enhancer-binding factor 1


Calculated molecular weight:

37 kDa


Observed molecular weight:

40-45 kDa


Gene symbol

LEF1


Synonyms

LEF 1, LEF1, TCF1 alpha, TCF1ALPHA

Background

Lymphoid enhancer-binding factor 1(LEF1) belongs to a family of regulatory protein share homology with high mobility group protein-1, and it’s a nuclear protein exprssed in pre-B and T cells. LEF1 has a role in the Wnt signaling pathway and hair cell differentiation and follicle morphogenesis. LEF1 exists as seven isoforms and we detects three isoforms with MW 44 kDa, 36 kDa and 23 kDa. Together with CTNNB1 and EP300, LEF1 activates transcription of target genes. Isoform 5 transcriptionally activates the fibronectin promoter, binds to and represses transcription from the E-cadherin promoter in a CTNNB1-independent manner, and is involved in reducing cellular aggregation and increasing cell migration of pancreatic cancer cells. Isoform 1 transcriptionally activates MYC and CCND1 expression and enhances proliferation of pancreatic tumor cells. MECs can give rise to seven cell types of the SAE and SMGs following severe airway injury. MECs progressively adopted a basal cell phenotype on the SAE and established lasting progenitors capable of further regeneration following reinjury. MECs activate Wnt-regulated transcription factors (Lef-1/TCF7) following injury and Lef-1 induction in cultured MECs promoted transition to a basal cell phenotype. Surprisingly, dose-dependent MEC conditional activation of Lef-1in vivopromoted self-limited airway regeneration in the absence of injury. Thus, modulating the Lef-1 transcriptional program in MEC-derived progenitors may have regenerative medicine applications for lung diseases. (https://doi.org/10.1016/j.stem.2018.03.017)The phosphorylation may affects LEF1 protein’s theoretical molecular weight when tested.40-60 kD bands have also been reported (PMID:22261717;17063141 ).

Protocols

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