CoraLite® Plus 488-conjugated ATP2A1 Recombinant monoclonal antibody

ATP2A1 Uni-rAb® Recombinant Antibody for IF-P
Cat No. CL488-84213-5

产品说明书

CloneNo. 241500D12

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

IF-P

241500D12, ATP2A, ATP2A 1, Calcium-transporting ATPase sarcoplasmic reticulum type, fast twitch skeletal muscle isoform, EC:7.2.2.10

缓冲液配方:  PBS, Proclin 300, BSA, Glycerol
PBS, Proclin 300, BSA, Glycerol
偶联物:  CoraLite® Plus 488
规格价格库存


经过测试的应用

Positive IF-P detected inmouse skeletal muscle tissue
For other applications, we recommend the unconjugated version of this antibody, 84213-5-PBS

推荐稀释比

应用推荐稀释比
Immunofluorescence (IF)-PIF-P : 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

CL488-84213-5 targets ATP2A1 in IF-P applications and shows reactivity with human, mouse, rat samples.

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

CatNo: Ag17944

Product name: Recombinant human ATP2A1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 561-635 aa of BC037354

Sequence: RCNYVRVGTTRVPLTGPVKEKIMAVIKEWGTGRDTLRCLALATRDTPPKREEMVLDDSARFLEYETDLTFVGVVG

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 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
别名 241500D12, ATP2A, ATP2A 1, Calcium-transporting ATPase sarcoplasmic reticulum type, fast twitch skeletal muscle isoform, EC:7.2.2.10
计算分子量 1001 aa, 110 kDa
观测分子量 110 kDa
GenBank蛋白编号BC037354
基因名称 ATP2A1
Gene ID (NCBI) 487
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 IDO14983
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

ATP2A1 also known as SERCA1, encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen and is involved in muscular excitation and contraction. Mutations in ATP2A1 cause some autosomal recessive forms of Brody disease(PMID: 23911890, 10914677).

实验方案

Product Specific Protocols
IF protocol for CL Plus 488 ATP2A1 antibody CL488-84213-5Download protocol
Standard Protocols
Click here to view our Standard Protocols
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