产品: ATPB 抗体
货号: DF12111
描述: Rabbit polyclonal antibody to ATPB
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Bovine, Horse, Rabbit, Chicken
分子量: 45-57 kDa; 57kD(Calculated).
蛋白号: P06576
RRID: AB_2844916

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   规格 价格 库存
 50ul RMB¥ 1250 现货
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Mouse,Rat
预测:
Pig(100%), Bovine(100%), Horse(100%), Rabbit(100%), Chicken(100%)
克隆:
Polyclonal
特异性:
ATPB Antibody detects endogenous levels of total ATPB.
RRID:
AB_2844916
引用格式: Affinity Biosciences Cat# DF12111, RRID:AB_2844916.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

ATP 5B; ATP synthase H+ transporting mitochondrial F1 complex beta polypeptide; ATP synthase subunit beta mitochondrial; ATP synthase subunit beta, mitochondrial; atp5b; ATPB; ATPB_HUMAN; ATPMB; ATPSB; Epididymis secretory protein Li 271; HEL-S-271; Mitochondrial ATP synthase beta subunit; Mitochondrial ATP Synthase Subunit Beta; Mitochondrial ATP synthetase beta subunit;

抗原和靶标

免疫原:
Uniprot:
基因/基因ID:
序列:
MLGFVGRVAAAPASGALRRLTPSASLPPAQLLLRAAPTAVHPVRDYAAQTSPSPKAGAATGRIVAVIGAVVDVQFDEGLPPILNALEVQGRETRLVLEVAQHLGESTVRTIAMDGTEGLVRGQKVLDSGAPIKIPVGPETLGRIMNVIGEPIDERGPIKTKQFAPIHAEAPEFMEMSVEQEILVTGIKVVDLLAPYAKGGKIGLFGGAGVGKTVLIMELINNVAKAHGGYSVFAGVGERTREGNDLYHEMIESGVINLKDATSKVALVYGQMNEPPGARARVALTGLTVAEYFRDQEGQDVLLFIDNIFRFTQAGSEVSALLGRIPSAVGYQPTLATDMGTMQERITTTKKGSITSVQAIYVPADDLTDPAPATTFAHLDATTVLSRAIAELGIYPAVDPLDSTSRIMDPNIVGSEHYDVARGVQKILQDYKSLQDIIAILGMDELSEEDKLTVSRARKIQRFLSQPFQVAEVFTGHMGKLVPLKETIKGFQQILAGEYDHLPEQAFYMVGPIEEAVAKADKLAEEHSS

种属预测

种属预测:

score>80的预测可信度较高,可尝试用于WB检测。*预测模型主要基于免疫原序列比对,结果仅作参考,不作为质保凭据。

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Chicken
100
Rabbit
100
Sheep
0
Dog
0
Xenopus
0
Zebrafish
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - P06576 作为底物

Site PTM Type Enzyme
T21 Phosphorylation
S23 Phosphorylation
S25 Phosphorylation
S51 Phosphorylation
K55 Ubiquitination
R109 Methylation
K124 Acetylation
K124 Ubiquitination
S128 Phosphorylation
K133 Acetylation
K133 Ubiquitination
T140 Phosphorylation
R155 Methylation
K159 Acetylation
K159 Ubiquitination
T185 Phosphorylation
Y196 Phosphorylation
K198 Acetylation
K198 Ubiquitination
K201 Ubiquitination
T213 Phosphorylation
Y230 Phosphorylation
S231 Phosphorylation
T240 Phosphorylation
Y247 Phosphorylation
K259 Acetylation
K259 Ubiquitination
K264 Ubiquitination
Y269 Phosphorylation
T288 Phosphorylation
Y292 Phosphorylation
T312 Phosphorylation
S316 Phosphorylation
S319 Phosphorylation
S327 Phosphorylation
T334 Phosphorylation
K350 Acetylation
K351 Ubiquitination
Y361 Phosphorylation
T374 Phosphorylation
Y395 Phosphorylation
S403 Phosphorylation
S415 Phosphorylation
Y418 Phosphorylation
K426 Acetylation
K426 Ubiquitination
K432 Methylation
S433 Phosphorylation
S447 Phosphorylation
S465 Phosphorylation
T475 Phosphorylation
K480 Acetylation
K480 Ubiquitination
K485 Acetylation
K485 Ubiquitination
K489 Ubiquitination
Y499 Phosphorylation
K519 Ubiquitination
K522 Acetylation
K522 Ubiquitination
S528 Phosphorylation
S529 Phosphorylation

研究背景

功能:

Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Subunits alpha and beta form the catalytic core in F(1). Rotation of the central stalk against the surrounding alpha(3)beta(3) subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.

细胞定位:

Mitochondrion inner membrane>Peripheral membrane protein>Matrix side.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
亚基结构:

F-type ATPases have 2 components, CF(1) - the catalytic core - and CF(0) - the membrane proton channel. CF(1) has five subunits: alpha(3), beta(3), gamma(1), delta(1), epsilon(1). CF(0) has three main subunits: a, b and c. Component of an ATP synthase complex composed of ATP5PB, ATP5MC1, ATP5F1E, ATP5PD, ATP5ME, ATP5PF, ATP5MF, MT-ATP6, MT-ATP8, ATP5F1A, ATP5F1B, ATP5F1D, ATP5F1C, ATP5PO, ATP5MG, ATP5MD and ATP5MPL. Interacts with PPIF. Interacts with BCL2L1 isoform BCL-X(L); the interaction mediates the association of BCL2L1 isoform BCL-X(L) with the mitochondrial membrane F(1)F(0) ATP synthase and enhances neurons metabolic efficiency. Interacts with CLN5 and PPT1.

蛋白家族:

Belongs to the ATPase alpha/beta chains family.

研究领域

· Human Diseases > Neurodegenerative diseases > Alzheimer's disease.

· Human Diseases > Neurodegenerative diseases > Parkinson's disease.

· Human Diseases > Neurodegenerative diseases > Huntington's disease.

· Metabolism > Energy metabolism > Oxidative phosphorylation.

· Metabolism > Global and overview maps > Metabolic pathways.

文献引用

1). Umbelliferone attenuates cisplatin-induced acute kidney injury by inhibiting oxidative stress and inflammation via NRF2. Physiological reports, 2023 (PubMed: 38030388) [IF=2.5]

Application: WB    Species: Mouse    Sample:

FIGURE 7 UMB (40 mg/kg) inhibited cisplatin‐induced oxidative stress by acting on NRF2 in mice. (a, b, c) Quantitative PCR was performed to analyze mRNA levels of renal HO‐1, SOD2, and ATP8. (d) Quantitative PCR analysis of mtDNA copy number in the kidneys of mice. 18S rDNA was used as an internal control. (e) Quantitative PCR was performed to analyze mRNA levels of renal PGC‐1α. (f) Western blot analysis of SOD2 and ATPB levels in the kidneys of each group of mice. (g & h) SOD2 and ATPB densitometry analysis. Data are shown as means ± standard deviation (n = 6 mice/group).

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