验证数据展示
经过测试的应用
Positive FC (Intra) detected in | HepG2 cells |
推荐稀释比
Application | Dilution |
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Flow Cytometry (FC) (INTRA) | FC (INTRA) : 0.80 ug per 10^6 cells in a 100 µl suspension |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
CL488-66852 targets XRN2 in FC (Intra) applications and shows reactivity with Human, mouse, rat samples.
Tested Applications | FC (Intra) Application Description |
Tested Reactivity | Human, mouse, rat |
Immunogen | XRN2 fusion protein Ag27927 种属同源性预测 |
Host / Isotype | Mouse / IgG1 |
Class | Monoclonal |
Type | Antibody |
Full Name | 5'-3' exoribonuclease 2 |
Synonyms | DHM1-like protein, DHM1 like protein, 5'-3' exoribonuclease 2, 5' 3' exoribonuclease 2, 5 3 exoribonuclease 2 |
Calculated Molecular Weight | 104 kDa |
Observed Molecular Weight | 109 kDa |
GenBank Accession Number | BC006417 |
Gene Symbol | XRN2 |
Gene ID (NCBI) | 22803 |
RRID | AB_3084279 |
Conjugate | CoraLite® Plus 488 Fluorescent Dye |
Excitation/Emission Maxima Wavelengths | 493 nm / 522 nm |
Form | Liquid |
Purification Method | Protein G purification |
UNIPROT ID | Q9H0D6 |
Storage Buffer | PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3. |
Storage Conditions | Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
XRN2 is one exonuclease that degrades the Pol II associated product of poly(A) site cleavage, which is crucial for Pol II termination. During transcription termination, XRN2 cleavages at the polyadenylation site liberates a 5' fragment which is subsequently processed to form the mature mRNA and a 3' fragment which remains attached to the elongating polymerase. The processive degradation of this 3' fragment by this protein may promote termination of transcription.
实验方案
Product Specific Protocols | |
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FC protocol for CL Plus 488 XRN2 antibody CL488-66852 | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |