anti-Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9) Antibodies

ACAD9 encodes a member of the acyl-CoA dehydrogenase family. Additionally we are shipping Acyl-CoA Dehydrogenase Family, Member 9 Proteins (2) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
ACAD9 28976 Q9H845
ACAD9 294973  
ACAD9 229211 Q8JZN5
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top anti-Acyl-CoA Dehydrogenase Family, Member 9 Antibodies at antibodies-online.com

Showing 10 out of 32 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Dog Rabbit Un-conjugated WB WB Suggested Anti-ACAD9 AntibodyTitration: 1.0 µg/mL <br /> Positive Control: 721_B Whole Cell 100 μL Log in to see 2 to 3 Days
$289.00
Details
Horse Rabbit Un-conjugated WB 50 μg Log in to see 7 to 9 Days
$551.83
Details
Human Rabbit Un-conjugated WB 100 μg Log in to see 2 to 3 Days
$245.00
Details
Human Rabbit Un-conjugated IC, IF, IHC, WB Immunofluorescent analysis of ACAD9 staining in MCF7 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody Immunohistochemical analysis of ACAD9 staining in human stomach formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the 200 μL Log in to see 13 to 14 Days
$487.50
Details
Human Rabbit Un-conjugated IF, IHC, WB Western blot analysis of extracts of various cells, using ACAD9 antibody. Immunohistochemistry of paraffin-embedded human stomach using ACAD9 antibody at dilution of 1:100 (x40 lens). 100 μL Log in to see 16 Days
$323.13
Details
Human Rabbit Un-conjugated ICC, IF, IHC, IHC (p), WB Immunohistochemistry-Paraffin: ACAD9 Antibody [NBP1-82749] - Immunohistochemical staining of human kidney shows strong granular cytoplasmic positivity in tubules. Immunocytochemistry/Immunofluorescence: ACAD9 Antibody [NBP1-82749] - Staining of human cell line A-431 shows positivity in mitochondria. 0.1 mL Log in to see 10 to 13 Days
$439.69
Details
Human Rabbit Un-conjugated WB Western Blot: ACAD9 Antibody [NBP1-74272] - 721_B Cell Lysate 1ug/ml Gel Concentration 12% 100 μL Log in to see 8 to 11 Days
$447.56
Details
Human Rabbit Un-conjugated ELISA, IHC   100 μL Log in to see 16 Days
$175.80
Details
Human Rabbit Un-conjugated ICC, IF, WB Immunocytochemistry/Immunofluorescence: ACAD9 Antibody  - Staining of human cell line A-431 shows localization to mitochondria. Western Blot: ACAD9 Antibody  - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma, human liver tissue and human tonsil tissue. 100 μL Log in to see 10 to 13 Days
$439.69
Details
Human Mouse Un-conjugated WB Western Blot analysis of ACAD9 expression in transfected 293T cell line by ACAD9 MaxPab polyclonal antibody.<br><br>Lane 1: ACAD9 transfected lysate(68.31 KDa).<br>Lane 2: Non-transfected lysate.<br> ACAD9 MaxPab polyclonal antibody. Western Blot analysis of ACAD9 expression in human liver. 50 μg Log in to see 11 to 12 Days
$430.00
Details

ACAD9 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human , ,
,

Rat (Rattus) , ,


Mouse (Murine) , ,


More Antibodies against Acyl-CoA Dehydrogenase Family, Member 9 Interaction Partners

Human Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9) interaction partners

  1. Study identified new mutations in ACAD9 responsible for a wide spectrum of heart diseases in the presence of elevated serum lactate levels.

  2. ACAD9 mutation is the most frequent cause of cardiac hypertrophy and isolated complex I deficiency.

  3. Case Report: neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.

  4. In cells where it is strongly expressed, ACAD9 plays a physiological role in fatty acid oxidation.

  5. Our results underscore the importance of the ACAD9 protein in complex I assembly and suggest that the enzymatic activity is a rudiment of the duplication event.

  6. Our data support a new function for ACAD9 in complex I function, making this gene an important new candidate for patients with complex I deficiency, which could be improved by riboflavin treatment.

  7. ACAD9 screening of 120 additional complex I-defective index cases led us to identify two additional unrelated cases and a total of five pathogenic ACAD9 alleles.

  8. Data show that two closely related metabolic enzymes, ACAD9 and VLCAD (show ACADVL Antibodies), diverged at the root of the vertebrate lineage to function in two separate mitochondrial metabolic pathways and have clinical implications for the diagnosis of complex I deficiency.

  9. Very high activity of CPT2 (show CPT2 Antibodies) and VCLAD, involved in the metabolism of long-chain fatty acids. Fatty acid oxidation may play role in energy generation in placenta, and deficiency in may result in placental dysfunction and gestational complications.

  10. ACAD9 may play a role in the turnover of lipid membrane unsaturated fatty acids that are essential for membrane integrity and structure

Mouse (Murine) Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9) interaction partners

  1. We conclude that disturbed mitochondrial bioenergetics in BAT (show BAAT Antibodies) is a critical contributing factor for the cold sensitivity in VLCAD (show ACADVL Antibodies) deficiency

Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9) Antigen Profile

Protein Summary

This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.

Gene names and symbols associated with ACAD9

  • acyl-CoA dehydrogenase family, member 9 (ACAD9) antibody
  • acyl-CoA dehydrogenase family, member 9 (Acad9) antibody
  • acyl-Coenzyme A dehydrogenase family, member 9 (Acad9) antibody
  • 2600017P15Rik antibody
  • 4732402K02 antibody
  • C630012L17Rik antibody
  • NPD002 antibody
  • Nyggf2 antibody

Protein level used designations for ACAD9

acyl-CoA dehydrogenase family member 9, mitochondrial , acyl-Coenzyme A dehydrogenase family, member 9 , very-long-chain acyl-CoA dehydrogenase VLCAD , ACAD-9 , very-long-chain acyl-CoA dehydrogenase VLCAD homolog

GENE ID SPECIES
28976 Homo sapiens
294973 Rattus norvegicus
229211 Mus musculus
Selected quality suppliers for anti-Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9) Antibodies
Did you look for something else?