官网链接
折扣/货期| 货号：GTX31949-PEP | 规格：50μg | 目录价：￥2400 |
产品详情
* 以下信息仅供参考，详情请以原厂网站为准
产品名称:
KIR2DS2 blocking peptide
别名:
Killer Cell Immunoglobulin Like Receptor, Two Ig Domains And Short Cytoplasmic Tail 2 , 183Acti , Cd158J , Cd158B , Kir-2Ds2 , Nkat-5 , Nkat5 , Cl-49 , Kir2Ds2
产品描述:
KIR2DS2 peptide is used for blocking the activity of KIR2DS2 antibody (catalog number GTX31949).
实验应用:
Neutralizing/Inhibition
克隆号:
偶联:
Unconjugated
产品浓度:
200 μg/ml (Please refer to the vial label for the specific concentration.)
保存温度:
Store as concentrated solution. Aliquot and store at -20ºC or below. Avoid freeze-thaw cycles.
运输温度:
dry ice
产品形式:
Liquid
存储溶液:
PBS, 0.1% BSA, 0.02% Sodium azide.
生产商:
GeneTex
功能与背景:
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several "framework" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are
您可能感兴趣的产品
ARFGAP1 Blocking Peptide
货号：33R-9999
Carbonic Anhydrase Vb Blocking Peptide (Mitochondrial)
货号：33R-9998
FBXL14 Blocking Peptide
货号：33R-9997
TMEM149 Blocking Peptide
货号：33R-9996
PLEKHH2 Blocking Peptide
货号：33R-9995
NECAP2 Blocking Peptide
货号：33R-9994
LARP7 Blocking Peptide
货号：33R-9993
UBE2L3 Blocking Peptide
货号：33R-9992
促销活动
精品推荐
复制QQ号成功，请打开QQ后添加好友进行咨询