- ￥8900
- GeneTex
- 美国
- GTX04393
- 2025年07月14日
- IHC-P
- Rabbit
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant fragment (around aa52-178) of human BL-CAM/CD22 protein
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX04393
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
IHC-P
- 浓度：
0.2 mg/ml (Please refer to the vial label for the specific concentration.)
- 抗体英文名：
CD22 antibody [MSVA-022R] HistoMAX
- 抗体名：
CD22 抗体 [MSVA-022R] HistoMAX
- 规格：
500 μl
IHC-P analysis of human spleen tissue section using GTX04393 CD22 antibody [MSVA-022R] HistoMAX.
CD22 positive B lymphocytes predominate in the white pulp but are only sparse in the red pulp.
IHC-P analysis of human B-cell chronic lymphocytic leukemia tissue section using GTX04393 CD22 antibody [MSVA-022R] HistoMAX.
B-CLL exhibiting strong CD22 staining of tumor cells.
IHC-P analysis of human ileum mucosa tissue section using GTX04393 CD22 antibody [MSVA-022R] HistoMAX.
CD22 positive B lymphocytes are rare in this sample of ileum mucosa.
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文献和实验Anti-CD22 Onconase: Preparation and Characterization
Antibodies can be conjugated to effector molecules to derive targeted therapeutics with properties such as cell-specific cytotoxicity. The murine anti-CD22 antibody RFB4 linked to a member of the ribonuclease A superfamily, Onconase (Onc
Mammalian Cell Display for Antibody Engineering
Antibody engineering has generally been carried out by displaying mouse or human antibodies or antibody fragments on the surface of microorganisms (phage, bacteria, and yeast). We have shown that mammalian cells can be used to display single
In Vitro Antibody Affinity Maturation Targeting Germline Hotspots
residues are most likely to have a major impact on antibody affinity. Here, we describe procedures for germline hotspot mutagenesis with an emphasis on strategies for randomizing hotspots with PCR and phage display, using as an example the anti-CD22
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