- ￥1880
- 晶风生物
- TF8605R
- 中国
- 2025年07月03日
- Elisa=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC=1:100-500,
- Rabbit
- Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,Guinea Pig,
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
神经毒性因子ICP34.5/人单纯疱疹病毒Ⅰ型抗体
- 抗体英文名：
HSV 1 Neurovirulence factor ICP34.5
- 靶点：
细胞浆 细胞膜 分泌型蛋白
- 浓度：
1mg/ml
- 应用范围：
Elisa=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC=1:100-500,
- 宿主：
Rabbit
- 适应物种：
Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,Guinea Pig,
- 保质期：
一年
- 抗原来源：
Rabbit
- 目录编号：
TF8605R
- 级别：
I级
- 库存：
10
- 供应商：
晶风生物
- 标记物：
FITC/Alexa/CY357/BIo/HRP
- 克隆性：
Polyclonal
- 保存条件：
-20
- 形态：
Liquid
- 亚型：
IgG
- 免疫原：
KLH conjugated synthetic peptide derived
- 规格：
50ul/100ul/200ul
产品规格：100ul/200ul(部分有50ul，如需更大包装或其他具体规格，请咨询客服)
研究领域：肿瘤 细胞生物 免疫学等
抗体来源：Rabbit
克隆类型：Polyclonal
交叉反应：Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,
产品应用：WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
性 状：Liquid
浓 度：1mg/ml
免 疫 原：KLH conjugated synthetic peptide derived
亚 型：IgG
纯化方法：affinity purified by Protein A
储 存 液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件：Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
HSV1NeurovirulencefactorICP34.5神经毒性因子ICP34.5/人单纯疱疹病毒Ⅰ型抗体相关抗体示例（非本抗体，如需本抗体，请联系客服索要说明书）：
Sample:
Liver (Mouse) Lysate at 40 ug
Spleen (Mouse) Lysate at 40 ug
NIH/3T3 (Mouse) CellLysate at 30 ug
RAW246.7 (Mouse) CellLysate at 30 ug
Primary: Anti- IL12 at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 22 kD
Observed band size: 35/36 kD
paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (IL12) Polyclonal Antibody, Unconjugated at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) instructions and DAB staining.
paraffin embedded (rat brain tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (IL12) Polyclonal Antibody, Unconjugated at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) instructionsand DAB staining.
HSV1NeurovirulencefactorICP34.5神经毒性因子ICP34.5/人单纯疱疹病毒Ⅰ型抗体
Blank control (blue line): Mouse spleen (blue).
Primary Antibody (green line): Rabbit Anti- IL12 antibody
Dilution: 1μg /10^6 cells;
Isotype Control Antibody (orange line): Rabbit IgG .
Secondary Antibody (white blue line): Goat anti-rabbit IgG-FITC
Dilution: 1μg /test.
Protocol
The cells were fixed with 70% ice-cold methanol overnight at 4℃. Cells stained with Primary Antibody for 30 min at room temperature. The cells were then incubated in 1 X PBS/2%BSA/10% goat serum to block non-specific protein-protein interactions followed by the antibody for 15 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
Tissue/cell: rat colitis tissue; paraffin-embedded;
Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,at 37℃ for 20 min;
Incubation: Anti-IL-12 Polyclonal Antibody, Unconjugated 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB staining
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文献和实验处理抗原的机制以及引起ＤＣ迁移和成熟的信号传导等领域研究的深入,有关人ＤＣ大量培养和扩增的方法日益成熟。目前,树突状细胞有三个来源:骨髓、外周血和新生儿脐带血。从骨髓中分离获得树突状细胞的ＣＤ+34的祖系细胞,或从外周血或新生儿脐带血于体外经14ｄ培养分化(在ＧＭＣＳＦ和ＴＮＦａ存在的情况下)成为成熟的ＣＤ+1ａ、ＣＤ+83、ＨＬＡＤＲ的树突状细胞;或者用外周血纯化的ＣＤ+14单核细胞或粘附单核细胞在二种细胞因子(ＧＭＣＳＦ和ＩＬ4或ＩＬ13)的培养刺激下成为ＣＤ+1ａ、ＣＤ+83的未成熟树突
网络 MHC抗原的结构及检测 MHC编码的抗原为一类同种异体抗原(alloantigen)。其中Ⅰ类和Ⅱ类抗原主要以细胞膜镶嵌蛋白的形式存在，也可脱落成为可溶性的形式。Ⅲ类抗原为补体C2、C4和B因子， 主要分泌到血清等体液中去。 一、MHC抗原的结构 (一)Ⅰ类抗原的结构和分布 Ⅰ类抗原由非共价键连接的两条多肽链组成，其中重链由MHCⅠ类基因编码，轻链
h,同上收集培养上清液 用双抗体夹心ELISA 方法测HSC-T6培养上清液中PⅢP ，CⅣ的含量。以上每组均设3个复孔，具体操作严格按照试剂盒说明进行。 1.3 统计学方法 采用SPSS12.0统计软件，进行Spearman相关分析，单因素ANOVA(方差分析)，两样本比较采用LSD-t检验，实验数据均以(x±s)表示,P＜0.05判定有显著性差异。 2 结果 2.1 HMGB1对 HSC-T6分泌PⅢP、CⅣ的剂量效应 HMGB1能促进
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