| 存储条件 |
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| Product Name | CD38 Recombinant Rabbit Monoclonal Antibody |
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| Antibody Type | Primary Antibodies |
| Immunogen | Synthetic peptide within human CD38 aa 250-300. |
| Clonality | Monoclonal |
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| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | FCICC/IFIF-PIHCWB |
| WB:1:1000 IHC:1:1000 ICC:1:50 IF-P:1:500 FC:1:1000 | |
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Purification | Protein A |
| Gene Symbol | CD38 |
|---|---|
| Gene Synonyms | ADPRC1 cADPR1 ADPRC 1 |
| Gene Full Name | CD38 molecule |
| Gene Summary | The protein encoded by this gene is a non-lineage-restricted, type II transmembrane glycoprotein that synthesizes and hydrolyzes cyclic adenosine 5'-diphosphate-ribose, an intracellular calcium ion mobilizing messenger. The release of soluble protein and the ability of membrane-bound protein to become internalized indicate both extracellular and intracellular functions for the protein. This protein has an N-terminal cytoplasmic tail, a single membrane-spanning domain, and a C-terminal extracellular region with four N-glycosylation sites. Crystal structure analysis demonstrates that the functional molecule is a dimer, with the central portion containing the catalytic site. It is used as a prognostic marker for patients with chronic lymphocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
| Alternative Names | Acute lymphoblastic leukemia cells antigen CD38 antibody ADP ribosyl cyclase 1 antibody ADP ribosyl cyclase antibody ADP ribosyl cyclase/cyclic ADP-ribose hydrolase antibody ADP-ribosyl cyclase 1 antibody ADPRC 1 antibody ADPRC1 antibody cADPr hydrolase 1 antibody CD 38 antibody CD38 antibody Acute lymphoblastic leukemia cells antigen CD38 antibody ADP ribosyl cyclase 1 antibody ADP ribosyl cyclase antibody ADP ribosyl cyclase/cyclic ADP-ribose hydrolase antibody ADP-ribosyl cyclase 1 antibody ADPRC 1 antibody ADPRC1 antibody cADPr hydrolase 1 antibody CD 38 antibody CD38 antibody CD38 antigen (p45) antibody CD38 antigen antibody CD38 molecule antibody Cd38-rs1 antibody CD38_HUMAN antibody CD38H antibody Cyclic ADP ribose hydrolase antibody Cyclic ADP ribose hydrolase 1 antibody Cyclic ADP-ribose hydrolase 1 antibody EC 3.2.2.5 antibody Ecto nicotinamide adenine dinucleotide glycohydrolase antibody I-19 antibody I19 (mouse) antibody Lymphocyte differentiation antigen CD38 antibody NAD(+) nucleosidase antibody NIM-R5 antigen antibody NIMR5 antigen (mouse) antibody OTTHUMP00000158633 antibody OTTHUMP00000217743 antibody p45 antibody T10 antibody |
| Molecular Weight(MW) | 34kDa(Observed band size: 45kDa) |
| Cellular Localization | Membrane. |
WB
Western blot analysis of CD38 on Daudi cell lysates with Rabbit anti-CD38 antibody at 1/1,000 dilution. Lysates/proteins at 10 µg/Lane. Predicted band size: 34 kDa Observed band size: 45 kDa Exposure time: 2 minutes; 12% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.
IHC
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-CD38 antibody at 1/2,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ICC/IF
Immunocytochemistry analysis of A549 cells labeling CD38 with Rabbit anti-CD38 antibody at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CD38 antibody at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
IF-P
Immunofluorescence analysis of paraffin-embedded human appendix tissue labeling CD38 with Rabbit anti-CD38 antibody at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 48) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
FC
Flow cytometric analysis of THP-1 cells labeling CD38. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).| Application Notes | WB:1:1000 IHC:1:1000 ICC:1:50 IF-P:1:500 FC:1:1000 |
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| Form | Liquid |
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| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
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