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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
peptide
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
-20℃
- 克隆性:
mAb
- 适应物种:
Human
- 保质期:
1年
- 目录编号:
TD-R50058
- 级别:
科研级
- 库存:
88
- 供应商:
武汉天德
- 宿主:
Rabbit
- 应用范围:
IHC-P
- 靶点:
详询
- 抗体英文名:
CD10
- 抗体名:
CD10
- 规格:
100ul/50ul/20ul
| 规格: | 100ul | 产品价格: | ¥2280.0 |
|---|---|---|---|
| 规格: | 50ul | 产品价格: | ¥1280.0 |
| 规格: | 20ul | 产品价格: | ¥658.0 |
CD10 Rabbit mAb
|
Product Name
|
CD10 Rabbit mAb
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|
Gene ID
|
4311
|
|
SwissProt ID
|
P08473
|
|
Gene Name
|
MME
|
|
Alternative Names
|
MME; EPN; Neprilysin; Atriopeptidase; Common acute lymphocytic leukemia antigen; CALLA; Enkephalinase; Neutral endopeptidase 24.11; NEP; Neutral endopeptidase; Skin fibroblast elastase; SFE; CD10
|
|
Background
|
CD10 is a transmembrane type II molecule and functions as a metallo-peptidase requiring zinc. Specifically, CD10 cleaves 1-3 amino-terminal amino acids from peptides with a preference for neutral amino acids (valine, iso-leucine, phenylalanine, leucine or alanine). Involved in the degradation of atrial natriuretic factor (ANF). Displays UV-inducible elastase activity toward skin preelastic and elastic fibers.
|
|
Research Field
|
Immunology
|
|
Product Categories
|
Pathological antibody
|
|
Host
|
Rabbit
|
|
Reactivity
|
Human
|
|
Application
|
IHC-P
|
|
Dilution Ratio
|
IHC: 1/100-1/200
|
|
Molecular Weight
|
-
|
|
Clonality
|
Monoclonal Antibody
|
|
Clonality No.
|
BP6059
|
|
Isotype
|
IgG
|
|
Immunogen
|
A synthesized peptide derived from human CD10
|
|
Purification
|
Affinity Purified
|
|
Conjugation
|
Unconjugated
|
|
Modification
|
Unmodified
|
|
Form
|
Liquid
|
|
Buffer System
|
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.
|
|
Storage
|
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
|
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文献和实验CD10 分子 CD10 常用单克隆抗体或代号:J5;(CALlA) 主要表达细胞:Pre-B,CAI。L,G[B] 分子质量(kDa)和结构:gp100(Ⅱ型膜分子) 功 能:为结合锌的金属蛋白酶,调节B细胞生长和增殖 CD10 Aka Common Acute Lymphoblastic Leukemia Antigen (CALLA), neutral endopeptidase 24.11, neprilysin
of patients with open heart surgery the expression of the membrane peptidases neprilysin/CD10 and aminopeptidase N/CD13, was determined on granulocytes in comparison to the monocytic HLA-DR expression. We used the QuantiBRITE™ flow cytometry
Generation of Dendritic Cells from Lymphoid Precursors
. Methods have become available to grow DC in culture, facilitating the study of their biological and developmental properties. One such method is described in this chapter to generate DC in vitro from CD34+ Lineage- (Lin- ) CD10+ bone marrow (BM) progenitor
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