Anti-Mouse CTLA-4/CD152 Rabbit Recombinant Antibody

CTLA-4/CD152 Uni-rAb® Recombinant Antibody for FC
Cat No. 98147-1-RR

产品说明书

CloneNo. 241100B8

宿主/亚型

Rabbit / IgG

种属反应性

mouse

应用

FC

Ctla4, Ly 56, Ctla 4, Cd152, 241100B8

缓冲液配方:  PBS, Azide
PBS, Azide
PBS Only
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive FC detected inCon A treated mouse splenocytes

推荐稀释比

应用推荐稀释比
Flow Cytometry (FC)FC : 0.25 ug per 10^6 cells in 100 μl suspension
This reagent has been tested for flow cytometric analysis. 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.

发表文章中的应用

FCSee 1 publications below

产品信息

98147-1-RR targets CTLA-4/CD152 in FC applications and shows reactivity with mouse samples.

经测试应用 FC Application Description
文献引用应用FC
经测试反应性 mouse
文献引用反应性mouse
免疫原

Fusion Protein

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Recombinant
产品类型 Antibody
全称 cytotoxic T-lymphocyte-associated protein 4
别名 Ctla4, Ly 56, Ctla 4, Cd152, 241100B8
计算分子量25 kDa
GenBank蛋白编号NM_009843.4
基因名称 CTLA-4
Gene ID (NCBI) 12477
RRIDAB_3672292
偶联类型 Unconjugated
形式Liquid
纯化方式Protein A purfication
UNIPROT IDP09793
储存缓冲液 PBS with 0.09% sodium azide, pH 7.3.
储存条件Store at 2 - 8°C. Stable for one year after shipment.

背景介绍

CTLA-4, also known as CD152, belonging to the immunoglobulin superfamily, is primarily found on activated T cells and regulatory T cells (Tregs). CTLA-4 is closely related to the T-cell costimulatory CD28, and both molecules bind to B7-1 and B7-2 on antigen-presenting cells. CTLA-4 acts as a negative regulatory molecule of T-cell responses. Besides the full-length transmembrane form, CTLA-4 also exists in a truncated soluble form (sCTLA-4).

实验方案

Product Specific Protocols
FC protocol for CTLA-4/CD152 antibody 98147-1-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
mouseFC

Nat Commun

Resistance to anti-LAG-3 plus anti-PD-1 therapy in head and neck cancer is mediated by Sox9+ tumor cells interaction with Fpr1+ neutrophils

Authors - Xiaochen Wang
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