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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
CD82 molecule
- 亚型:
IgG2a
- 形态:
liquid
- 保存条件:
负20摄氏度
- 克隆性:
monoclonal
- 标记物:
Non-conjugated
- 适应物种:
Human, mouse
- 保质期:
6个月
- 抗原来源:
Mouse
- 目录编号:
Q9BZJ3
- 级别:
纯化级别
- 库存:
50
- 供应商:
LSM bio
- 宿主:
E. coli - derived recombinant protein
- 应用范围:
ELISA, WB, IHC
- 浓度:
≥95% as determined by SDS-PAGE
- 靶点:
CD82 molecule
- 抗体英文名:
CD82 antibody
- 抗体名:
CD82 antibody
- 规格:
100μl
CD82 antibody
Product Name CD82 antibody
Catalog No PAab09921
Packing 100ul
Form liquid
Alternative Name 4F9, C33, C33 antigen, CD82, CD82 antigen, CD82 molecule, GR15, IA4, Inducible membrane protein R2, KAI1, Metastasis suppressor Kangai 1, R2, SAR2, ST6, Tetraspanin 27, Tspan 27, TSPAN27
Purification protein A+G purified
Purity 95% as determined by SDS-PAGE
Host Mouse
Isotype IgG2a
Storage PBS with 0.02% sodium azide and 50% glycerol pH 7.3 , -20Centigrade for 24 months (Avoid repeated freeze / thaw cycles.)
Background/ FUNCTION
Immunogen CD82 molecule
Specificity Human, mouse
Tested Application ELISA, WB, IHC
Recommended dilution WB: 1:1000-1:4000; IHC: 1:1000-1:3000
IHC use Immunohistochemistry of paraffin-embedded human tonsillitis tissue slide using PAab09921 (CD82 antibody) at dilution of 1:2000
WB use
Jurkat cells were subjected to SDS PAGE followed by western blot with PAab09921 (CD82 antibody) at dilution of 1:2000
Protein Information
Gene ID 3732
Uniprot ID P27701
Calculated MW 48 kDa
Research Area Cancer, Immunology, Signal Transduction
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文献和实验CD82 分子 CD82 常用单克隆抗体或代号: 1A4,4F9;(R2) 主要表达细胞: Leu [B] 分子质量(kDa)和结构: gp50- 53(TM4-SF) 功 能: 淋巴细胞活化,信号传递 CD82 Aka prostate cancer antimetastasis gene KAI1, kang ai (Chinese for anticancer).
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera
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