Recombinant CD68 Monoclonal Antibody (AN301076L)

For research use only.
Verified Samples |
Verified Samples in WB: U-87MG Verified Samples in IHC: Human liver tissue |
Dilution | IHC 1:1000-5000, WB 1:1000-5000 |
Isotype | IgG,κ |
Host | Rabbit |
Reactivity | Human |
Applications | WB, IHC |
Clonality | Monoclonal;Recombinant |
Immunogen | Recombinant Human CD68 protein |
Abbre | CD68 |
Synonyms | SRD, LAMP, DKFZp686M, MACROPHAGE ANTIGEN CD, CD68 antigenmacrophage antigen CD, Scavenger receptor class D member, SR-D, SCARD, CD68, GP110, LAMP4, SCARD1, CD 68, CD68 antigen, CD68 antigenmacrophage antigen CD68, CD68 molecule, DKFZp686M18236, gp11, MACROPHAGE ANTIGEN CD68, Macrophage antigen CD68 (microsialin), Macrosialin, Scavenger receptor class D member 1, SRD1, SR-D1, gp110, CD 68, CD68, CD68 antigen, CD68 molecule, CD68, DKFZp686M18236, gp11, Gp110, LAMP4, Macrophage antigen CD68 (microsialin), MACROPHAGE ANTIGEN CD68, Macrosialin, SCARD1, Scavenger receptor class D member 1 |
Swissprot | |
Calculated MW | 35 kDa |
Observed MW |
120 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 | Membranous |
Concentration | 0.2 mg/mL |
Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
Purification Method | Protein A |
Research Areas | Immunology |
Clone No. | 1F16 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | Ice bag |
background | This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages. It is a member of the lysosomal/endosomal-associated membrane glycoprotein (LAMP) family. The protein primarily localizes to lysosomes and endosomes with a smaller fraction circulating to the cell surface. It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue- and organ-specific lectins or selectins. The protein is also a member of the scavenger receptor family. Scavenger receptors typically function to clear cellular debris, promote phagocytosis, and mediate the recruitment and activation of macrophages. Alternative splicing results in multiple transcripts encoding different isoforms. |
Other Clones
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Unconjugated
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