Abnova

UNC13D Monoclonal Antibody (2C7)

Name: UNC13D Monoclonal Antibody (2C7)
Brand: Abnova
SKU: H00201294-M05
Availability: InStock

查看其他11个Munc13-4抗体

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

Additional Information:

抗体检测数据 (1)

图: 1 / 1

UNC13D Antibody (H00201294-M05) in WB

UNC13D monoclonal antibody (M05), clone 2C7. Western Blot analysis of UNC13D expression in Jurkat.

Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.

Product Image Gallery

Immunogen image

Immunogen Image UNC13D Monoclonal Antibody (2C7)

产品信息

H00201294-M05

应用

建议稀释比

已发表文章

免疫印迹 (WB)

1-5 µg/mL

酶联免疫吸附实验 (ELISA)

10 µg/mL

产品规格

种属反应

Human, Mouse

宿主/亚型

Mouse / IgG2a, kappa

分类

Monoclonal

类型

Antibody

克隆号

2C7

抗原

UNC13D (NP_954712.1, 2 a.a. approximately 100 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

3D表位/免疫原

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

0.5 mg/mL

100 µg

纯化类型

Protein A

保存液

PBS, pH 7.4

内含物

no preservative

保存条件

-20°C, Avoid Freeze/Thaw Cycles

运输条件

Ambient (domestic); Wet ice (international)

产品详细信息

Product may be used with Western Blot (Cell lysate).

Immunogen sequence: ATLLSHPQQR PPFLRQAIKI RRRRVRDLQD PPPQMAPEIQ PPSHHFSPEQ RALLYEDALY TVLHRLGHPE PNHVTEASEL LRYLQEAFHV EPEEHQQTL

靶标信息

This gene encodes a protein that is a member of the UNC13 family, containing similar domain structure as other family members but lacking an N-terminal phorbol ester-binding C1 domain present in other Munc13 proteins. The protein appears to play a role in vesicle maturation during exocytosis and is involved in regulation of cytolytic granules secretion. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive disorder.

仅用于科研。不用于诊断过程。未经明确授权不得转售。