CoraLite® Plus 647-conjugated FOXG1 Recombinant monoclonal antibody

FOXG1 Uni-rAb® Recombinant Antibody for IF/ICC
Cat No. CL647-85930

产品说明书

CloneNo. 250144E8

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

IF/ICC

FOXG 1, BF-1, BF-2, forkhead box G1, Forkhead box protein G1

缓冲液配方:  PBS, Proclin 300, BSA, Glycerol
PBS, Proclin 300, BSA, Glycerol
偶联物:  CoraLite® Plus 647
规格价格库存


经过测试的应用

Positive IF/ICC detected inU-251 cells, C6 cells
For other applications, we recommend the unconjugated version of this antibody, 85930-1-PBS

推荐稀释比

应用推荐稀释比
Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
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.

产品信息

CL647-85930 targets FOXG1 in IF/ICC applications and shows reactivity with human, mouse, rat samples.

经测试应用 IF/ICC Application Description
经测试反应性 human, mouse, rat
免疫原

CatNo: Ag17169

Product name: Recombinant human FOXG1 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 190-489 aa of BC035020

Sequence: IMMAIRQSPEKRLTLNGIYEFIMKNFPYYRENKQGWQNSIRHNLSLNKCFVKVPRHYDDPGKGNYWMLDPSSDDVFIGGTTGKLRRRSTTSRAKLAFKRGARLTSTGLTFMDRAGSLYWPMSPFLSLHHPRASSTLSYNGTTSAYPSHPMPYSSVLTQNSLGNNHSFSTANGLSVDRLVNGEIPYATHHLTAAALAASVPCGLSVPCSGTYSLNPCSVNLLAGQTSYFFPHVPHPSMTSQSSTSMSARAASSSTSPQAPSTLPCESLRPSLPSFTTGLSGGLSDYFTHQNQGSSSNPLIH

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 forkhead box G1
别名 FOXG 1, BF-1, BF-2, forkhead box G1, Forkhead box protein G1
计算分子量 489 aa, 52 kDa
观测分子量60 kDa
GenBank蛋白编号BC035020
基因名称 FOXG1
Gene ID (NCBI) 2290
偶联类型 CoraLite® Plus 647 Fluorescent Dye
最大激发/发射波长654 nm / 674 nm
形式Liquid
纯化方式Protein A purification
UNIPROT IDP55316
储存缓冲液 PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
储存条件Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

Forkhead Box G1 (FOXG1) is a member of the Forkhead family of genes with non-redundant roles in brain development, where alteration of this gene's expression significantly affects the formation and function of the mammalian cerebral cortex. FOXG1 haploinsufficiency in humans is associated with prominent differences in brain size and impaired intellectual development noticeable in early childhood, while homozygous mutations are typically fatal.

实验方案

Product Specific Protocols
IF protocol for CL Plus 647 FOXG1 antibody CL647-85930Download protocol
Standard Protocols
Click here to view our Standard Protocols
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