CoraLite® Plus 488-conjugated SURF1 Recombinant antibody

SURF1 Uni-rAbTM Recombinant Antibody for FC (Intra)
Cat No. CL488-83052-6

产品说明书

CloneNo. 230210E12

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

FC (Intra)

Surfeit locus protein 1, surfeit 1, SURF-1, SURF 1, 230210E12

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  CoraLite® Plus 488
规格: 

-/ -


经过测试的应用

Positive FC (Intra) detected inHepG2 cells
For other applications, we recommend the unconjugated version of this antibody, 83052-6-PBS

推荐稀释比

应用推荐稀释比
Flow Cytometry (FC) (INTRA)FC (INTRA) : 0.80 ug per 10^6 cells in a 100 µl suspension
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

CL488-83052-6 targets SURF1 in FC (Intra) applications and shows reactivity with human samples.

经测试应用 FC (Intra) Application Description
经测试反应性 human
免疫原 SURF1 fusion protein Ag3959 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 surfeit 1
别名 Surfeit locus protein 1, surfeit 1, SURF-1, SURF 1, 230210E12
计算分子量 33 kDa
观测分子量30-31 kDa
GenBank蛋白编号BC028314
基因名称 SURF1
Gene ID (NCBI) 6834
RRIDAB_3673175
偶联类型 CoraLite® Plus 488 Fluorescent Dye
最大激发/发射波长493 nm / 522 nm
形式 Liquid
纯化方式Protein A purification
UNIPROT IDQ15526
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

SURF1 (Surfeit locus protein 1), also known as SURF-1. It is expected to be located in mitochondrion inner membrane, which is ubiquitinated in thyroid and kidney. This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. The molecular weight of SURF1 is 33 kDa.

实验方案

Product Specific Protocols
FC protocol for CL Plus 488 SURF1 antibody CL488-83052-6Download protocol
Standard Protocols
Click here to view our Standard Protocols
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