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200μL $ 410.00
120μL $ 260.00
60μL $ 160.00
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For research use only.

Verified Samples Verified Samples in WB: Mouse heart, Mouse lung, Mouse kidney, Mouse brain, Rat heart, Rat lung, Rat brain
Verified Samples in IHC: Mouse pancreas
Verified Samples in IF: Rat pancreas
Dilution WB 1:500-1:2000,  IHC 1:200-1:400
Isotype IgG
Host Rabbit
Reactivity Mouse,  Rat
Applications WB,  IHC,  IF
Clonality Polyclonal
Immunogen KLH conjugated Synthetic peptide corresponding to Mouse PDGFB
Abbre PDGFB
Synonyms Becaplermin,  PDGF 2,  PDGF B chain,  PDGF subunit B,  PDGF-2,  PDGF2,  PDGFB,  Pdgfb,  Platelet derived growth factor 2,  Platelet-derived growth factor B chain,  Platelet-derived growth factor beta polypeptide,  Platelet-derived growth factor subunit B,  Proto-oncogene c-Sis,  S
Calculated MW 27 kDa
Observed MW 27 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 Endoplasmic reticulum, endoplasmic reticulum lumen, Extracellular region or secreted, extracellular matrix, extracellular region, extracellular space, Golgi apparatus, Golgi lumen, Golgi membrane, Plasma Membrane, basolateral plasma membrane, Other locations: cell surface, cytoplasm, platelet alpha granule lumen.
Concentration 410 μg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 1% protein protectant and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cardiovascular,  Metabolism,  Developmental Biology,  Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a motif of eight cysteines. This gene product can exist either as a homodimer (PDGF-BB) or as a heterodimer with the platelet-derived growth factor alpha polypeptide (PDGF-AB), where the dimers are connected by disulfide bonds. Mutations in this gene are associated with meningioma. Reciprocal translocations between chromosomes 22 and 7, at sites where this gene and that for COL1A1 are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans resulting from unregulated expression of growth factor. Two alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
Other Clones

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Unconjugated

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