- ￥2260
- LSM Bio
- 进口
- PAab09987
- 2025年07月13日
- ELISA, WB, IHC
- E. coli - derived recombinant protein
- Human, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
heat shock 70kDa protein 5
- 亚型：
IgG
- 形态：
liquid
- 保存条件：
负20摄氏度
- 克隆性：
polyclonal
- 标记物：
Non-conjugated
- 适应物种：
Human, Rat
- 保质期：
6个月
- 抗原来源：
Rabbit
- 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：
heat shock 70kDa protein 5
- 抗体英文名：
HSPA5 antibody
- 抗体名：
HSPA5 antibody
- 规格：
100μl
HSPA5 antibody
Product Name HSPA5 antibody
Catalog No PAab09987
Packing 100ul
Form liquid
Alternative Name BIP, GRP 78, GRP78, HSP A5, HSPA5, MIF2
Purification Immunogen affinity purified
Purity 95% as determined by SDS-PAGE
Host Rabbit
Isotype IgG
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 heat shock 70kDa protein 5
Specificity Human, Rat
Tested Application ELISA, WB, IHC
Recommended dilution WB: 1:500-1:2000; IHC: 1:50-1:500
IHC use Immunohistochemistry of paraffin-embedded human pancreas cancer using PAab09987(HSPA5 antibody) at dilution of 1:200
WB use
HeLa cells were subjected to SDS PAGE followed by western blot with PAab09987(HSPA5 antibody) at dilution of 1:1000
Protein Information
Gene ID 3309
Uniprot ID P11021
Calculated MW 78 kDa
Research Area
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文献和实验with chaperones in these cells is of interest. Furthermore, Pb and Cu bind strongly to the molecular chaperone heat shock 70 kDa protein Hspa5, also known as glucose-regulated protein 78 (Grp78) or immunoglobulin-binding protein (BiP). This chapter describes
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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