Recombinant S100A8 Monoclonal Antibody (AN300035P)
For research use only.
| Verified Samples | Verified Samples in WB:HL-60 |
| Dilution | WB: 1:1000；IHC-P: 1:200-1:1000；IP: 1:20-1:50 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | WB, IHC-P, IP |
| Clonality | Recombinant;Monoclonal |
| Immunogen | Recombinant Human S100A8 protein |
| Abbre | S100A8 |
| Synonyms | Protein S100-A, S100a, Kcnip, KCHIP, MRP, S100A8, 60B8AG, CAGA, CFAG, CGLA, CP-10, L1Ag, MA387, MIF, MRP8, NIF, P8, Calgranulin A, Calgranulin-A, Cystic fibrosis antigen, Leukocyte L1 complex light chain, MRP-8, Protein S100-A8, CALP, KCNIP4, KCHIP4, AI323541, B8Ag, BEE11, Calprotectin, Calprotectin L1L subunit, Chemotactic cytokine CP-10, included, Migration inhibitory factor-related protein 8, Myeloid-related protein 8, Neutrophil cytosolic 7 kDa protein, Pro-inflammatory S100 cytokine, S100 calcium binding protein A8, S100 calcium binding protein A8 (calgranulin A), S100 calcium-binding protein A8, S100A8/S100A9 complex, S10A8, Urinary stone protein band A |
| Swissprot | |
| Calculated MW | 11 kDa |
| Observed MW |
11 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. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Neuroscience, Cancer, Immunology, Signal Transduction, Cell Biology, Epigenetics and Nuclear Signaling |
| Clone | A1145 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | This gene (IFNGR1) encodes the ligand-binding chain (alpha) of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection. In addition , defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease , also known as familial disseminated atypical mycobacterial infection. [provided by RefSeq , Jul 2008] , |
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