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Recombinant Phospho-Cyclin D1 (Thr286) Monoclonal Antibody (AN301503L)

Recombinant Phospho-Cyclin D1 (Thr286) Monoclonal Antibody - 1
  • Recombinant Phospho-Cyclin D1 (Thr286) Monoclonal Antibody - 1
  • Recombinant Phospho-Cyclin D1 (Thr286) Monoclonal Antibody - 2
  • Recombinant Phospho-Cyclin D1 (Thr286) Monoclonal Antibody - 3
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All Size Price Qty
100μL $ 380.00
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50μL $ 249.00
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For research use only.

Verified Samples Verified Samples in WB: HT-1080
Verified Samples in IHC: Human endometrial cancer, Human esophagus, Mouse pancreas, Rat pancreas
Verified Samples in FCM: MCF-7
Dilution WB 1:500-1:2000,  IHC 1:50-1:100,  FCM 1:50
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Rat,  Mouse
Applications WB,  IHC,  FCM
Clonality Monoclonal;Recombinant
Immunogen Recombinant human Phospho-Cyclin D1 (Thr286) fragment
Abbre Phospho-Cyclin D1 (Thr286)
Synonyms Cyl,  PRAD,  U21B,  CCND,  B cell leukemia,  G1/S specific cyclin D,  Cyclin D,  BCL,  BCL1,  D11S287E,  PRAD1,  U21B31,  CCND1,  Cyclin D1,  B cell leukemia 1,  BCL 1,  Cd1,  Cyl 1,  G1/S specific cyclin D1,  BCL1,  D11S287E,  PRAD1,  U21B31,  CCND1,  Cyclin D1,  cyclin D1
Swissprot
Calculated MW 34 kDa
Observed MW 34 kDa

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Nucleus, Cytoplasm
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Cell Biology,  Epigenetics and Nuclear Signaling,  Cancer
Clone No. A202
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background Regulatory component of the cyclin D1-CDK4 (DC) complex that phosphorylates and inhibits members of the retinoblastoma (RB) protein family including RB1 and regulates the cell-cycle during G1/S transition. Cyclin D-CDK4 complexes are major integrators of various mitogenenic and antimitogenic signals. Also substrate for SMAD3, phosphorylating SMAD3 in a cell-cycle-dependent manner and repressing its transcriptional activity. Component of the ternary complex, cyclin D1/CDK4/CDKN1B, required for nuclear translocation and activity of the cyclin D-CDK4 complex. Exhibits transcriptional corepressor activity with INSM1 on the NEUROD1 and INS promoters in a cell cycle-independent manner.
Other Clones

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Unconjugated

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