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Catalog Number | orb1787819 |
---|---|
Category | Antibodies |
Description | Affinity Purified Rabbit Polyclonal Antibody (Pab) |
Species/Host | Rabbit |
Clonality | Polyclonal |
Tested applications | FC, IHC-P, WB |
Reactivity | Human |
Isotype | Rabbit IgG |
Immunogen | 737-763 aa |
Dilution range | WB: 1:1000, WB: 1:1000, WB: 1:500-1:2000, IHC-P: 1:10~50, FC: 1:10~50 |
Form/Appearance | 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. |
Conjugation | Unconjugated |
MW | 83000 Da |
Target | This HADHA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 737-763 amino acids from the C-terminal region of human HADHA. |
UniProt ID | P40939 |
NCBI | NP_000173.2 |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles |
Alternative names | Trifunctional enzyme subunit alpha, mitochondrial, Read more... |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
HADHA Antibody (C-term) western blot analysis in A431 cell line lysates (35 ug/lane). This demonstrates the HADHA antibody detected the HADHA protein (arrow).
HADHA Antibody (C-term) flow cytometry analysis of Ramos cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
Formalin-fixed and paraffin-embedded human lung carcinoma reacted with HADHA Antibody (C-term), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
All lanes: Anti-HADHA Antibody (C-term) at 1:1000 dilution. Lane 1: Hela whole cell lysate. Lane 2: Jurkat whole cell lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 83 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.
A predominant 75 kDa band for the HEK293T wild type lysate was observed (3 ug/ml anti-HADHA) vs the predicted size of 83 kDa. The molecular weight discrepancy could be due to post-translationally modification of the target protein, a splice-variant form of the target protein, a partially degraded form of the target protein, or an unrelated protein which shares the antibody-reactive epitope. A less intense band at 65 kDa was also A weak band only in the 20ug lane was observed for the knock out lysate, suggesting incomplete knockout of the target gene.