Facebook
Toll-free:1-888-852-8623

All categories

  • All categories
  • Flow Cytometry Antibodies
  • ELISA Kits
  • MACS Cell Isolation
  • Antibodies and Reagents
  • Apoptosis and Cell Health Detection
  • Metabolism Assays
  • Immunoassays
  • Cell Identification Kits
  • Proteins and Peptides
  • Cell Culture
Please enter the item number/product keyword!
Keyword cannot be empty !
INSERT SYMBOLS:
  • α
  • β
  • γ
  • δ
  • ε
  • ζ
  • η
  • θ
  • κ
  • μ
  • ω
  • σ
  • τ
  • λ
  • ⅩⅢ
  • ⅩⅢ
  • ⅩⅣ
  • ⅩⅤ
  • ⅩⅦ
  • ⅩⅧ
  • UP ↑
Recombinant HNF-1B Monoclonal Antibody - 1
  • Recombinant HNF-1B Monoclonal Antibody - 1
  • Recombinant HNF-1B Monoclonal Antibody - 2
  • Recombinant HNF-1B Monoclonal Antibody - 3
All Size Price Qty
100μL $ 380.00
- +
50μL $ 249.00
- +
Add to cart

For research use only.

Verified Samples Verified Samples in WB: Jurkat, Mouse liver, Rat liver
Dilution WB 1:2000-1:10000
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Rat,  Mouse
Applications WB
Clonality Monoclonal;Recombinant
Immunogen Recombinant human HNF-1B fragment
Abbre HNF-1B
Synonyms LFB,  HNF,  HPC,  LF-B,  MODY,  VHNF,  TCF,  HNF1B,  FJHN,  HNF-1-beta,  HNF-1B,  HNF1beta,  HNF2,  HPC11,  LF-B3,  LFB3,  MODY5,  TCF-2,  TCF2,  VHNF1,  Hepatocyte nuclear factor 1 beta,  Hepatocyte nuclear factor 1-beta,  HNF 1B,  HNF 2,  HNF1 beta,  HNF1 homeobox B,  Homeoprotein LF B3,  Homeoprotein LFB3,  LF B3,  MODY 5,  TCF 2,  TCF 2 protein,  TCF2 protein,  Transcription factor 2,  Transcription factor 2 hepatic,  Variant hepatic nuclear factor,  Variant hepatic nuclear factor 1,  VHNF 1
Swissprot
Calculated MW 61 kDa
Observed MW 61 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
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Epigenetics and Nuclear Signaling,  Metabolism
Clone No. A434
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background Hepatocyte nuclear factor 1-beta (HNF-1B) is a transcription factor which binds to specific regions of nucleic acid. HNF-1B, which plays critical roles in the regulation of glucose transport and metabolism, glucose-stimulated insulin secretion, and also in the embryonic development and later function of the pancreas, kidneys, genitourinary tract, liver, and the biliary tree.
Other Clones

{{antibodyDetailsPage.numTotal}} Results

Other Formats

{{formatDetailsPage.numTotal}} Results

Unconjugated

  • IF:{{item.impact}}

    Journal:{{item.journal}} ({{item.year}})

    DOI:{{item.doi}}

    Reactivity:{{item.species}}

    Sample Type:{{item.organization}}

  • Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}

Product Information