Product Name
CYB5R3, Polyclonal Antibody
Full Product Name
CYB5R3 Antibody
Product Synonym Names
B5R; DIA1
Product Gene Name
anti-CYB5R3 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Species Reactivity
Human, Mouse, Rat
Purity/Purification
Antigen affinity purification
Immunogen
Fusion protein of CYB5R3
Calculated Molecular Weight: 33kd
Observed Molecular Weight: 30-35kd
Buffer
PBS with 0.1% sodium azide and 50% glycerol pH 7.3.
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-68062 / sc-68063 / sc-67284
Preparation and Storage
Store at -20 degree C. Avoid freeze / thaw cycles
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.
Other Notes
Small volumes of anti-CYB5R3 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-CYB5R3 antibody
ELISA (EIA), Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
Application Notes for anti-CYB5R3 antibody
WB: 1:500-1:5000
IHC: 1:20-1:200
IF: 1:20-1:50
Testing Data of anti-CYB5R3 antibody
NCBI/Uniprot data below describe general gene information for CYB5R3. It may not necessarily be applicable to this product.
NCBI Accession #
CAK54725.1
[Other Products]
UniProt Secondary Accession #
O75675; Q8TDL8; Q8WTS8; Q9UEN4; Q9UEN5; Q9UL55; Q9UL56; B1AHF2; B7Z7L3[Other Products]
UniProt Related Accession #
P00387[Other Products]
Molecular Weight
38,226 Da
NCBI Official Full Name
CYB5R3, partial
NCBI Official Synonym Full Names
cytochrome b5 reductase 3
NCBI Official Symbol
CYB5R3??[Similar Products]
NCBI Official Synonym Symbols
B5R; DIA1
??[Similar Products]
NCBI Protein Information
NADH-cytochrome b5 reductase 3; NADH-cytochrome b5 reductase 3 membrane-bound form; NADH-cytochrome b5 reductase 3 soluble form; diaphorase-1
UniProt Protein Name
NADH-cytochrome b5 reductase 3
UniProt Synonym Protein Names
Diaphorase-1Cleaved into the following 2 chains:NADH-cytochrome b5 reductase 3 membrane-bound form; NADH-cytochrome b5 reductase 3 soluble form
Protein Family
NADH-cytochrome b5 reductase
UniProt Gene Name
CYB5R3??[Similar Products]
UniProt Synonym Gene Names
DIA1; B5R; Cytochrome b5 reductase??[Similar Products]
UniProt Entry Name
NB5R3_HUMAN
NCBI Summary for CYB5R3
This gene encodes cytochrome b5 reductase, which includes a membrane-bound form in somatic cells (anchored in the endoplasmic reticulum, mitochondrial and other membranes) and a soluble form in erythrocytes. The membrane-bound form exists mainly on the cytoplasmic side of the endoplasmic reticulum and functions in desaturation and elongation of fatty acids, in cholesterol biosynthesis, and in drug metabolism. The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is involved in methemoglobin reduction. The membrane-bound form has both membrane-binding and catalytic domains, while the soluble form has only the catalytic domain. Alternate splicing results in multiple transcript variants. Mutations in this gene cause methemoglobinemias. [provided by RefSeq, Jan 2010]
UniProt Comments for CYB5R3
CYB5R3: Desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction. Defects in CYB5R3 are the cause of methemoglobinemia CYB5R3-related (METHB-CYB5R3). A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia. There are two types of methemoglobinemia CYB5R3-related. In type 1, the defect affects the soluble form of the enzyme, is restricted to red blood cells, and causes well- tolerated methemoglobinemia. In type 2, the defect affects both the soluble and microsomal forms of the enzyme and is thus generalized, affecting red cells, leukocytes and all body tissues. Type 2 methemoglobinemia is associated with mental deficiency and other neurologic symptoms. Belongs to the flavoprotein pyridine nucleotide cytochrome reductase family. 3 isoforms of the human protein are produced by alternative promoter.
Protein type: Carbohydrate Metabolism - amino sugar and nucleotide sugar; Oxidoreductase; Mitochondrial; EC 1.6.2.2
Chromosomal Location of Human Ortholog: 22q13.2
Cellular Component: endoplasmic reticulum membrane; mitochondrial outer membrane; mitochondrion; membrane; endoplasmic reticulum; hemoglobin complex; cytoplasm; mitochondrial inner membrane; lipid particle
Molecular Function: FAD binding; cytochrome-b5 reductase activity; ADP binding; NAD binding; AMP binding
Biological Process: vitamin metabolic process; blood circulation; L-ascorbic acid metabolic process; cholesterol biosynthetic process; water-soluble vitamin metabolic process
Disease: Methemoglobinemia Due To Deficiency Of Methemoglobin Reductase
Research Articles on CYB5R3
1. A comprehensive overview of the study of structure and function of human cytochrome b5 reductase.
Precautions
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