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现在位置首页>实验试剂制品>抗体>抗体>Abcam ab13857 Rabbit polyclonal to Rb 200ul
Abcam ab13857 Rabbit polyclonal to Rb 200ul
Abcam ab13857 Rabbit polyclonal to Rb 200ul
  • Abcam ab13857 Rabbit polyclonal to Rb 200ul

Abcam ab13857 Rabbit polyclonal to Rb 200ul

产品报价:询价

更新时间:2013/6/20 13:23:01

地:美国

牌:Abcam

号: ab13857

厂商性质: 生产型,贸易型,服务型,

公司名称: 上海盈东生物科技有限公司

产品关键词:

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Overview

Product name

Anti-Rb antibody
参阅全部 Rb 抗体 (46) ...

Description

Rabbit polyclonal to Rb

Tested applications

WBmore details

Cross reactivity

 

Reacts with

Mouse, Rat, Human

 

Immunogen

Synthetic peptide: RTPRRGQNRSARIAKQLE, corresponding to amino acids 251-268 of Human Rb.

RTPRRGQNRSARIAKQLE

Positive control

Jurkat whole cell lysate.

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

Storage buffer

Preservative: 0.05% Sodium Azide
Constituents: 0.2% Gelatin, PBS

Concentration

 

  • 200 µl

 

Purity

Protein G purified

Clonality

Polyclonal

Isotype

IgG

Research areas

Cancer >> Oncoproteins/suppressors >> Tumor suppressors >> Rb family
Cancer >> Oncoproteins/suppressors >> Tumor suppressors
Epigenetics and Nuclear Signaling >> Transcription >> Cancer susceptibility >> Tumor Suppressors
Cell Biology >> Cell Cycle >> Cell Cycle Inhibitors >> Rb
 

  • Datasheet PDF
  • Western blot - Anti-Rb antibody (ab13857)Western blot - Anti-Rb antibody (ab13857) image(enlarge)

Applications

Show applications key

Our Abpromise guarantee covers the use of ab13857 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • ShowHide1 Image

    WB

    WB: 1/200 - 1/1000. Dete...Read more →

    WB: 1/200 - 1/1000. Detects a band of approximately 110 kDa (predicted molecular weight: 110 kDa).

Target

Function

Key regulator of entry into cell division that acts as a tumor suppressor. Acts as a transcription repressor of E2F1 target genes. The underphosphorylated, active form of RB1 interacts with E2F1 and represses its transcription activity, leading to cell cycle arrest. Directly involved in heterochromatin formation by maintaining overall chromatin structure and, in particular, that of constitutive heterochromatin by stabilizing histone methylation. Recruits and targets histone methyltransferases SUV39H1, SUV420H1 and SUV420H2, leading to epigenetic transcriptional repression. Controls histone H4 'Lys-20' trimethylation. Inhibits the intrinsic kinase activity of TAF1. Mediates transcriptional repression by SMARCA4/BRG1 by recruiting a histone deacetylase (HDAC) complex to the c-FOS promoter. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex (By similarity). In case of viral infections, interactions with SV40 large T antigen, HPV E7 protein or adenovirus E1A protein induce the disassembly of RB1-E2F1 complex thereby disrupting RB1's activity.

Tissue specificity

Expressed in the retina.

Involvement in disease

Defects in RB1 are the cause of childhood cancer retinoblastoma (RB) [MIM:180200]. RB is a congenital malignant tumor that arises from the nuclear layers of the retina. It occurs in about 1:20'000 live births and represents about 2% of childhood malignancies. It is bilateral in about 30% of cases. Although most RB appear sporadically, about 20% are transmitted as an autosomal dominant trait with incomplete penetrance. The diagnosis is usually made before the age of 2 years when strabismus or a gray to yellow reflex from pupil ('cat eye') is investigated.
Defects in RB1 are a cause of susceptibility to bladder cancer (BLC) [MIM:109800]. A malignancy originating in tissues of the urinary bladder. It often presents with multiple tumors appearing at different times and at different sites in the bladder. Most bladder cancers are transitional cell carcinomas. They begin in cells that normally make up the inner lining of the bladder. Other types of bladder cancer include squamous cell carcinoma (cancer that begins in thin, flat cells) and adenocarcinoma (cancer that begins in cells that make and release mucus and other fluids). Bladder cancer is a complex disorder with both genetic and environmental influences.
Defects in RB1 are a cause of osteogenic sarcoma (OSRC) [MIM:259500].

Sequence similarities

Belongs to the retinoblastoma protein (RB) family.

Domain

The Pocket domain binds to the threonine-phosphorylated domain C, thereby preventing interaction with heterodimeric E2F/DP transcription factor complexes.

Post-translational
modifications

Phosphorylated in G1, thereby releasing E2F1 which is then able to activate cell growth. Dephosphorylated at the late M phase. SV40 large T antigen, HPV E7 and adenovirus E1A bind to the underphosphorylated, active form of pRb. Phosphorylation at Thr-821 and Thr-826 promotes interaction between the C-terminal domain C and the Pocket domain, and thereby inhibits interactions with heterodimeric E2F/DP transcription factor complexes. Dephosphorylated at Ser-795 by calcineruin upon calcium stimulation.
N-terminus is methylated by METTL11A/NTM1 (By similarity). Monomethylated at Lys-860 by SMYD2, promoting interaction with L3MBTL1.

Cellular localization

Nucleus.

Information by UniProt

Alternative names

  • Including osteosarcoma antibody
  • OSRC antibody
  • Osteosarcoma antibody
see all

Database links

  • Entrez Gene: 5925 Human
  • Entrez Gene: 19645 Mouse
  • Entrez Gene: 24708 Rat
  • Omim: 614041 Human
  • SwissProt: P06400 Human
  • SwissProt: P13405 Mouse
  • SwissProt: P33568 Rat
  • Unigene: 408528 Human
see all

Anti-Rb antibody images:

Western blot - Anti-Rb antibody (ab13857)

Western blot - Anti-Rb antibody (ab13857)

 

 



Predicted band size : 110 kDa


Western blot analysis of Rb in 30 mgs of Jurkat cell lysate using ab13857 at 1:1000 dilution.