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CoraLite®568-conjugated ATP5A1 Monoclonal antibody
ATP5A1 Monoclonal Antibody for
Host / Isotype
Mouse / IgG2b
Reactivity
human, mouse, rat, monkey
Applications
Conjugate
CoraLite®568 Fluorescent Dye
CloneNo.
1B10H3
验证数据展示
Planning an IHC experiment? We recommend our IHCeasy ATP5A1 Ready-To-Use IHC Kit. ATP5A1 primary antibody included.
For other applications, we recommend the unconjugated version of this antibody, 66037-1-Ig
产品信息
CL568-66037 targets ATP5A1 in applications and shows reactivity with human, mouse, rat, monkey samples.
| Tested Applications | Application Description |
| Tested Reactivity | human, mouse, rat, monkey |
| Immunogen | ATP5A1 fusion protein Ag8119 种属同源性预测 |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Full Name | ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle |
| Synonyms | ATP5A 1, ATP5A, ATP synthase F1 subunit alpha, 1B10H3 |
| Calculated Molecular Weight | 60 kDa |
| GenBank Accession Number | BC064562 |
| Gene Symbol | ATP5A1 |
| Gene ID (NCBI) | 498 |
| RRID | AB_2919718 |
| Conjugate | CoraLite®568 Fluorescent Dye |
| Excitation/Emission Maxima Wavelengths | 568 nm / 587 nm |
| Form | Liquid |
| Purification Method | Protein A purification |
| UNIPROT ID | P25705 |
| Storage Buffer | PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3. |
| Storage Conditions | Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
The ATP5A1 gene encodes the α subunit of mitochondrial ATP synthase which produces ATP from ADP in the presence of a proton gradient across the membrane. The mitochondrial ATP synthase, also known as Complex V or F1F0 ATP synthase, is a multi-subunit enzyme complex consisting of two functional domains, the F1-containing the catalytic core and the Fo- containing the membrane proton channel. F0 domain has 10 subunits: a, b, c, d, e, f, g, OSCP, A6L, and F6. F1 is composed of subunits α, β, γ, δ, ε, and a loosely attached inhibitor protein IF1. Recently defect in ATP5A1 has been linked to the fatal neonatal mitochondrial encephalopathy. ATP5A1 is localized in the mitochondria and anti-ATP5A1 can be used as the loading control for mitochondrial or Complex V proteins. This antibody recognizes the endogenous ATP5A1 protein in lysates from various cell lines and tissues. The predicted MW of ATP5A1 is 60 kDa, while it undergoes the transit peptide cleavage to become a mature form around 50-55 kDa. Several isoforms of ATP5A1 exist due to the alternative splicing.
