产品: CEACAM8 抗体
货号: DF10151
描述: Rabbit polyclonal antibody to CEACAM8
应用: WB IHC IF/ICC
文献应用: IF/ICC
反应: Human, Rat
分子量: 38 kDa; 38kD(Calculated).
蛋白号: P31997
RRID: AB_2840730

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   规格 价格 库存
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:1000-3000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Rat
克隆:
Polyclonal
特异性:
CEACAM8 Antibody detects endogenous levels of total CEACAM8.
RRID:
AB_2840730
引用格式: Affinity Biosciences Cat# DF10151, RRID:AB_2840730.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

Carcinoembryonic antigen CGM6; Carcinoembryonic antigen gene family member 6; Carcinoembryonic antigen related cell adhesion molecule 8; Carcinoembryonic antigen-related cell adhesion molecule 8; CD 66b; CD 67; CD66b; CD66b antigen; CD67; CD67 antigen; CEACAM 8; CEACAM8; CEAM8_HUMAN; CGM 6; CGM6; NCA 95; NCA95; Non-specific cross-reacting antigen NCA-95; Nonspecific cross reacting antigen NCA 95; Nonspecific cross reacting antigen NCA95;

抗原和靶标

免疫原:
Uniprot:
基因/基因ID:
表达:
P31997 CEAM8_HUMAN:

Expressed in leukocytes of chronic myeloid Leukemia patients and bone marrow.

序列:
MGPISAPSCRWRIPWQGLLLTASLFTFWNPPTTAQLTIEAVPSNAAEGKEVLLLVHNLPQDPRGYNWYKGETVDANRRIIGYVISNQQITPGPAYSNRETIYPNASLLMRNVTRNDTGSYTLQVIKLNLMSEEVTGQFSVHPETPKPSISSNNSNPVEDKDAVAFTCEPETQNTTYLWWVNGQSLPVSPRLQLSNGNRTLTLLSVTRNDVGPYECEIQNPASANFSDPVTLNVLYGPDAPTISPSDTYYHAGVNLNLSCHAASNPPSQYSWSVNGTFQQYTQKLFIPNITTKNSGSYACHTTNSATGRNRTTVRMITVSDALVQGSSPGLSARATVSIMIGVLARVALI

翻译修饰 - P31997 作为底物

Site PTM Type Enzyme
Y120 Phosphorylation
K126 Methylation
N288 N-Glycosylation
S296 Phosphorylation

研究背景

功能:

Cell surface glycoprotein that plays a role in cell adhesion in a calcium-independent manner. Mediates heterophilic cell adhesion with other carcinoembryonic antigen-related cell adhesion molecules, such as CEACAM6. Heterophilic interaction with CEACAM8 occurs in activated neutrophils.

翻译修饰:

Glycosylated.

细胞定位:

Cell membrane>Lipid-anchor. Cell surface.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
组织特异性:

Expressed in leukocytes of chronic myeloid Leukemia patients and bone marrow.

亚基结构:

Monomer. Heterodimer with CEACAM6; heterodimerizes via its Ig-like V-type domain.

蛋白家族:

The N-terminus Ig-like V-type domain is necessary for heterophilic intercellular adhesion.

Belongs to the immunoglobulin superfamily. CEA family.

文献引用

1). Neutrophil extracellular traps induce a hypercoagulable state in glioma. Immunity Inflammation and Disease, 2021 (PubMed: 34288521) [IF=3.2]

Application: IF/ICC    Species: Human    Sample: glioma tissues

FIGURE 2 Platelet‐neutrophil interaction triggers NET generation in glioma patients. (A) Control neutrophils were incubated with PLT‐rich plasma from glioma patients and healthy subjects and stained with MPO (red) and DAPI (blue). (B) Plasma from stage III/IV glioma patients activated neutrophils to release higher proportions of NETs than those from stage I/II glioma patients and healthy subjects. (C) Immunofluorescence images also showed PLTs (CD41, green) decorated on DNA traps (DAPI, blue) when neutrophils (CD66b, red) were incubated with plasma from glioblastoma (GBM; stage IV glioma) patients. (D) PLT‐neutrophil aggregates, defined as CD41+/CD66b+ cells, were investigated in samples from each group. (E) The rate of PLT‐neutrophil aggregates was highest in samples from GBM patients. (F) Control neutrophils were incubated with PLTs from glioma patients and healthy subjects and analyzed by immunofluorescence microscopy. PLTs from stage III/IV glioma patients, especially GBM patients, were potent activators of NET formation than those from stage I/II glioma patients and healthy subjects. (G, H) Anti‐P‐selectin and PSGL‐1 antibodies were used to inhibit the interaction between neutrophils and PLTs and the NET (propidium iodide, red) formation was markedly decreased. The scale bar in (A) and (G) is 20 μm and (C) is 80μm. The results are expressed as the mean±SD. *p<.05, **p<.01, ***p<.001, and ****p<.0001. DAPI, 4′,6‐diamidino‐2‐ phenylindole; MPO, myeloperoxidase; NET, neutrophil extracellular trap; PLT, platelet

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