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Rabbit Anti-ACADM antibody
Rabbit Anti-ACADM antibody
mitochondrial antibody; ACAD 1; ACAD1; Acyl coenzyme A dehydrogenase; Acyl coenzyme A dehydrogenase C 4 to C 12 straight chain; MCAD; MCADH; Medium chain acyl CoA dehydrogenase; Medium chain fatty acyl CoA dehydrogenase; Medium chain specific acyl CoA deh
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Regular members: $476.8
  • NO.:SLM-60484R
    Clonality:Monoclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,Rat
    Applications:WB,IHC-P,IHC-F,ICC/IF,IF,Flow-Cyt
    concentration:1mg/ml
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Product Name ACADM
Chinese Name 酰基辅酶A脱氢酶中链Recombinant rabbit monoclonal anti
Alias mitochondrial antibody; ACAD 1; ACAD1; Acyl coenzyme A dehydrogenase; Acyl coenzyme A dehydrogenase C 4 to C 12 straight chain; MCAD; MCADH; Medium chain acyl CoA dehydrogenase; Medium chain fatty acyl CoA dehydrogenase; Medium chain specific acyl CoA dehydrogenase; Medium chain specific acyl CoA dehydrogenase mitochondrial; FLJ18227; FLJ93013; FLJ99884; ACADM_HUMAN.
Immunogen Species Rabbit
Clonality Monoclonal
Clone NO. H5A10
React Species Human,Mouse,Rat
Applications WB=1:500-2000,IHC-P=1:50-200,IHC-F=1:50-200,ICC/IF=1:50-200,IF=1:50-200,Flow-Cyt=1:50-100(Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Cellular localization The cell membrane
Form Liquid
Concentration 1mg/ml
Lsotype IgG/Kappa
Purification Affinity purified by Protein A
Buffer Solution 1M TBS(pH7.4) with 1% BSA, 3% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Subcellular Location:
Mitochondrion matrix.

SWISS:
P11310

Gene ID:
34

Database links:

Entrez Gene: 34 Human

SwissProt: P11310 Human



酰基辅酶,是一种特殊的酰基链长度为4-16的脱氢酶,它催化脂肪酸β氧化的起始步骤。利用电子转移黄蛋白(ETF)作为电子受体,通过ETF-泛醌氧化还原酶(ETF脱氢酶)将电子转移到Mitochondrion呼吸链。
Product Picture
Blocking buffer: 5% NFDM/TBST
Primary ab dilution: 1:1000
Primary ab incubation condition: 2 hours at room temperature
Secondary ab: Goat Anti-Rabbit IgG H&L (HRP)
Lysate: HeLa, HepG2
Protein loading quantity: 20 μg
Exposure time: 30 s
Predicted MW: 45 kDa
Observed MW: 45 kDa
Cell line: HeLa
Fixative: 100% Ice-cold methanol
Permeabilization: 0.1% TritonX-100
Primary ab dilution: 1:50
Primary incubation condition: 4°C overnight
Secondary ab: Goat Anti-Rabbit IgG
Nuclear counter stain: DAPI (Blue)
Comment: Color green is the positive signal for SLM-60484R

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