Comparison

RBL5

Item no. 18-272-196691
Manufacturer GENWAY
Amount 0.1 mg
Category
Type Antibody
Applications WB, IP, IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-43A3DE
Similar products 18-272-196691
Available
Genway ID:
GWB-43A3DE
Isotype:
IgG
Immunogen:
Synthetic peptide (Human) (C terminal).
Antigen Species:
Human
Target:
RBL5
Localization:
Nuclear
Concentration:
0. 2 mg/ml Storage
Preservative:
0. 1% Sodium Azide. Constituents: 0. 2% Gelatin PBS
Application Note:
IHC-Fr: Use at an assay dependent dilution. IP: Use at an assay dependent dilution. WB: 1/200. Predicted
Molecular Weight:
130 kDa. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular
Localization:
Nuclear Two retinoblastoma related proteins p107 and pRb2 / p130 which are structurally and functionally similar to the product of the retinoblastoma gene (pRb / p105) were cloned by taking advantage of their ability to bind transforming proteins of DNA tumor viruses through a particular region called the \" pocket domain. \" Like pRb both proteins play a fundamental role in growth control. These Rb family proteins were measured in a variety of lung neoplasms. The highest percentage of undetectable levels and the tightest inverse correlation with the histological grading and with PCNA expression in the most aggressive tumor types were found for pRb2 / p130 which may suggest an important role for this protein in the pathogenesis and progression of lung cancer.
Function:
Key regulator of entry into cell division. 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 SUV420H1 and SUV420H2 leading to epigenetic transcriptional repression. Controls histone H4 \' Lys-20\' trimethylation. Probably acts as a transcription repressor by recruiting chromatin-modifying enzymes to promoters. Potent inhibitor of E2F-mediated trans-activation associates preferentially with E2F5. Binds to cyclins A and E. Binds to and may be involved in the transforming capacity of the adenovirus E1A protein. May act as a tumor suppressor.
Subunit:
Interacts with AATF. Interacts with SUV420H1 and SUV420H2 (By similarity). Component of the DREAM complex (also named LINC complex) at least composed of E2F4 E2F5 LIN9 LIN37 LIN52 LIN54 MYBL1 MYBL2 RBL1 RBL2 RBBP4 TFDP1 and TFDP2. The complex exists in quiescent cells where it represses cell cycle-dependent genes. It dissociates in S phase when LIN9 LIN37 LIN52 and LIN54 form a subcomplex that binds to MYBL2. Interacts with RINT1.
Subcellular Location:
Nucleus.
Ptm:
During G0 and early G1 phase of the cell cycle phosphorylated on Ser-639 and on 5 sites within the domain B. Phosphorylation on Ser-672 in G1 leads to its ubiquitin-dependent proteolysis.
Miscellaneous:
G0-restricted expression.
Similarity:
Belongs to the retinoblastoma protein (RB) family.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.1 mg
Available: In stock
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