BD-PB0975-PABPN1L Rabbit Polyclonal Antibody (Center)-现货抗体产品库武汉枢密脑科学技术有限公司

PABPN1L Rabbit Polyclonal Antibody (Center)

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产品基本信息

产品货号

BD-PB0975

产品名称

PABPN1L Rabbit Polyclonal Antibody (Center)

别名

Embryonic polyadenylate-binding protein 2, Embryonic poly(A)-binding protein 2, ePABP-2, ePABP2, Embryonic poly(A)-binding protein type II, Poly(A)-binding protein nuclear-like 1, PABPN1L, EPABP2, PABPNL1

类别

常规抗体

推荐应用

反应种属

Human

Human Gene ID

NP_001073956.2

Human Swissprot No.

A6NDY0

特异性

This PABPN1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 166-194 amino acids from the Central region of human PABPN1L.

稀释度

WB~~1:500-1:1000;IHC-P~~1:100~500;IF~~1:10~50;FC~~1:10~50

预测分子量

30kDa

同种型

Rabbit Ig

背景介绍

The function of this protein remains unknown.

组织表达

Expressed in various adult tissues.

细胞定位

Cytoplasm.

期货

现货

纯化

Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.

All lanes : Anti-PABPN1L Antibody (Center) at 1:500-1:1000 dilution Lane 1: A549 whole cell lysate Lane 2: human kidney lysate Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size : 30 kDa Blocking/Dilution buffer: 5% NFDM/TBST.

PABPN1L Antibody (Center)immunohistochemistry analysis in formalin fixed and paraffin embedded human liver tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of PABPN1L Antibody (Center) for immunohistochemistry. Clinical relevance has not been evaluated.

Confocal immunofluorescent analysis of PABPN1L Antibody (Center) with A549 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

PABPN1L Antibody (Center) flow cytometric analysis of A549 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.