Cat.No | MBA-0005 |
Name | Rabbit anti-5-HT (Serotonin) 5A Receptor Antibody |
中文名字 | 兔抗-5-HT 5A受体抗体,兔抗血清素抗体 |
Description | The 5-HT5A Receptor was quality control tested using standard immunohisto-chemical methods. The antiserum demonstrates strongly positive labeling of rat cortex and hippocampus using indirect immunofluorescent and biotin/avidin-HRP techniques. Recommended primary dilution is 1/200 – 1/400 in PBS/0.3% Triton X-100 – Bn/Av-HRP. Intensification methods such as nickel will approximately double the dilution factor as recommended. |
Clonality | Polyclonal |
Isotype | IgG |
Host | Rabbit |
Quantity/Volume | 50ul/100 µL |
State | Liquid |
Reacts With | Clam, Rat |
Preabsorption Control | / |
Alternate Names | 5-hydroxytryptamine receptor 5A; 5-HT5A; REC17; 5ht5a,MR22; 5-hydroxytryptamine (serotonin) receptor 5A, G protein-coupled, anti-5-HT5a |
RRID | AB_572213 |
Immunogen | This information is proprietary to Mabioway |
Gene Symbol | Htr5a |
Entrez Gene ID | Entrez Gene: 25689 Rat |
NCBI Gene Aliases | / |
Sequence | >sp|P47898|5HT5A_HUMAN 5-hydroxytryptamine receptor 5A |
APPLICATION | |
Quality Control | The ImmunoStar 5-HT5A Receptor was quality control tested using standard immunohistochemical methods. The antiserum demonstrates significant labeling of rat cortex and hippocampus using indirect immunofluorescent and biotin/avidin-HRP techniques. Intensification methods such as nickel will approximately double the dilution factor as recommended. The antibody was characterized by immunoblotting and immunohistochemistry. Immunoblots of rat brain extracts revealed the presence of two bands at molecular weights of 41 and 47 kD. The lower weight band agrees with the calculated molecular weight based on amino acid sequence. The higher weight may represent glycosylated receptor protein. Due to the difficulty with receptor antibodies, western blot applications are not warranted and are included as specificity information only. Immunohistochemical staining of rat brain correlates well with Northern blot analysis and in situ hybridization studies. Immunolabeling is completely abolished by preadsorption with synthetic rat 5-HT5A receptor (17–34). |
Tissue | Rat cortex and hippocampus |
Perfusion Fixation | • Fixative - 4% paraformaldehyde in 0.1M Phosphate buffer, pH 7.4; 500 mL over 20 min. |
Absorption Control | / |
Sections | 10 µm cryostat or 50 µm vibratome |
Tissue Incubation | 48 hours at 2°–8° C. |
Detection System | Use Cy3 or Bn/AV-HRP reagents at dilutions recommended by the manufacturer. |
Suggested Dilution | 1/100–1/300 in PBS/0.3% Triton X-100 – Bn/AV-HRP immunohistochemistry |
NOTES | |
Special Instructions | It is recommended that the researcher perform a primary antibody dilution series using our dilution recommendations as a guideline. Note that a change in the fixation or buffering system from our protocol may change the configuration of the protein which could alter the reactivity with the tissue tested. |
Concentration | Not applicable. Antibody concentration is only relevant for purified antibodies. |
Storage | Store at 2°–8°C until expiration date. |