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eCl@ss:
32160702
UNSPSC Code:
12352203
NACRES:
NA.46
Conjugate:
unconjugated
Clone:
1D9.2, monoclonal
Application:
immunohistochemistry
western blot
western blot
Species reactivity:
human
Citations:
Technique(s):
immunohistochemistry: suitable (paraffin)
western blot: suitable
western blot: suitable
Uniprot accession no.:
产品名称
Anti-CYB5R3 Antibody, clone 1D9.2, clone 1D9.2, from mouse
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
1D9.2, monoclonal
species reactivity
human
technique(s)
immunohistochemistry: suitable (paraffin)
western blot: suitable
isotype
IgG2aκ
NCBI accession no.
UniProt accession no.
shipped in
ambient
target post-translational modification
unmodified
Quality Level
Gene Information
human ... CYB5R3(1727)
Analysis Note
Evaluated by Western Blotting in HepG2 celll lysate.
Western Blotting Analysis: 0.5 µg/mL of this antibody detected CYB5R3 in 10 µg of HepG2 cell lysate.
Western Blotting Analysis: 0.5 µg/mL of this antibody detected CYB5R3 in 10 µg of HepG2 cell lysate.
Application
Detect CYB5R3 using this mouse monoclonal Anti-CYB5R3 Antibody, clone 1D9.2, Cat. No. MABS1727, validated for use in Immunohistochemistry (Paraffin) and Western Blotting.
Immunohistochemistry Analysis: A 1:250 dilution from a representative lot detected CYB5R3 in human kidney, skeletal muscle, and tonsil tissue sections.
Biochem/physiol Actions
Target epitope is present in both the ER/mitochondria membrane-bound and cytosolic forms of human CYB5R3.
General description
NADH-cytochrome b5 reductase 3 (EC 1.6.2.2; UniProt P00387; also known as B5R, Cytochrome b5 reductase, Diaphorase-1) is encoded by the CYB5R3 (also known as DIA1) gene (Gene ID 1727) in human. Cytochrome b5 reductase is a flavoprotein that serves as electron donor for cytochrome b5, a ubiquitous electron carrier and participates in a variety of metabolic pathways, including desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction. It is produced as two different isoforms that have different localizations. The membrane-bound form is found in somatic cells where it is anchored to the endoplasmic reticulum and mitochondrial membranes. The soluble form is found in erythrocytes. Mutations in the CYB5R3 gene result in deficiency in NADH-cytochrome b5 reductase+C20 in erythrocytes, which causes methemoglobinemia types I and II that are characterized by the presence of excessive amounts of methemoglobin in blood cells and their reduced capacity to carry oxygen. Ref.: Elahian, F., et al. (2014). Crit. Rev Biotechnol. 34, 134-143.
~34 kDa observed. 34.10 kDa (isoform 1 or M; Membrane-bound form with Met1 removed, a.a. 2-301), 31.26 kDa (Cytosolic form, a.a. 27-301), 31.63 kDa (isoform 2 or S), 38.23 kDa (isoform 3) calculated. Uncharacterized bands may be observed in some lysate(s).
Immunogen
GST-tagged recombinant human CYB5R3 C-terminal fragment.
Other Notes
Concentration: Please refer to lot specific datasheet.
Physical form
Format: Purified
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
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