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The antibody against CHDH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 245-594 of human CHDH (NP_060867.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.
The antibody against CHDH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 245-594 of human CHDH (NP_060867.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.
Western blot analysis of various lysates, using CHDH Rabbit pAb at 1:1000 dilution.
Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Negative control (NC):Jurkat
Exposure time: 1s.
| Cat.No | ADA-00216A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | CHDH |
| Target Synonyms | CHDH | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse kidney, 293T, HepG2, Mouse liver, Mouse pancreas, Mouse testis, Mouse thymus, Rat kidney | Application | ELISA, WB, IHC-P |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 245-594 of human CHDH (NP_060867.2). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q8NE62 | Immunogen Sequence |
Uniprot Id
Q8NE62
Target Species
Human
Target Name
CHDH
Target Full Name
Choline dehydrogenase, mitochondrial
Target Subcellular Location
Mitochondrion inner membrane.
Target Protein Families
GMC oxidoreductase family
Target Synonyms
CDH; CHD; CHDH; CHDH_HUMAN; Choline dehydrogenase; mitochondrial
Target Background
The protein encoded by this gene is a choline dehydrogenase that localizes to the mitochondrion. Variations in this gene can affect susceptibility to choline deficiency. A few transcript variants have been found for this gene, but the full-length nature of only one has been characterized to date.
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