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Recombinant B7-H3/CD276 Monoclonal Antibody (AN301442L)

Recombinant B7-H3/CD276 Monoclonal Antibody - 1
  • Recombinant B7-H3/CD276 Monoclonal Antibody - 1
  • Recombinant B7-H3/CD276 Monoclonal Antibody - 2
  • Recombinant B7-H3/CD276 Monoclonal Antibody - 3
  • +8
All Size Price Qty
100μL $ 380.00
- +
50μL $ 249.00
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For research use only.

Verified Samples Verified Samples in WB: HeLa, MCF-7, 293T
Verified Samples in IHC: Human cervical cancer, Human lung squamous carcinoma, Human tonsil, Mouse spleen, Mouse stomach
Verified Samples in IF: HeLa, THP-1
Verified Samples in FCM: THP-1, HeLa
Verified Samples in IP: HeLa cells extracts
Dilution WB 1:500-1:2000,  IHC 1:200-1:1000,  IF 1:50,  FCM 1:50-1:100,  IP 1:25-1:100
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Mouse
Applications WB,  IHC,  IF,  FCM,  IP
Clonality Monoclonal;Recombinant
Immunogen Recombinant human B7-H3/CD276 fragment
Abbre B7-H3/CD276
Synonyms B7H,  UNQ,  PRO,  B7-H,  B7RP,  B7 homolog,  B7H34Ig-B7-H,  PSEC,  4Ig-B7-H,  CD276,  4Ig-B7-H3,  B7-H3,  B7H3,  B7RP-2,  B7 homolog 3,  B7H34Ig-B7-H3,  CD276 antigen,  CD276 molecule,  Costimulatory molecule,  PSEC0249,  UNQ309,  PRO352,  B7RP-2,  4Ig-B7-H3,  B7H3,  B7-H3,  CD276 antigen
Swissprot
Calculated MW 57 kDa
Observed MW 110 kDa
The actual band is not consistent with the expectation.

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 Membrane
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Immunology,  Cancer,  Stem Cells
Clone No. A137
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background May participate in the regulation of T-cell-mediated immune response. May play a protective role in tumor cells by inhibiting natural-killer mediated cell lysis as well as a role of marker for detection of neuroblastoma cells. May be involved in the development of acute and chronic transplant rejection and in the regulation of lymphocytic activity at mucosal surfaces. Could also play a key role in providing the placenta and fetus with a suitable immunological environment throughout pregnancy. Both isoform 1 and isoform 2 appear to be redundant in their ability to modulate CD4 T-cell responses. Isoform 2 is shown to enhance the induction of cytotoxic T-cells and selectively stimulates interferon gamma production in the presence of T-cell receptor signaling.
Other Clones

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Unconjugated

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