IdnK antibody (AA 56-182) (Biotin)
Quick Overview for IdnK antibody (AA 56-182) (Biotin) (ABIN7999038)
Target
See all IdnK (IDNK) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 56-182
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Purpose
- Anti-IDNK Antibody Biotin Conjugated
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Predicted Reactivity
- Human IDNK shares 70.9% amino acid (aa) sequence identity with both mouse,rat IDNK.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human IDNK recombinant protein (Position: Q56-E182). Human IDNK shares 70.9% amino acid (aa) sequence identity with both mouse and rat IDNK.
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Isotype
- IgG
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Application Notes
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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Expiry Date
- 12 months
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- IdnK (IDNK) (IdnK Gluconokinase Homolog (IDNK))
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Alternative Name
- IDNK
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Background
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Background: C9orf103 (chromosome 9 open reading frame 103), also known as gluconate kinase, is a 187 amino acid protein that belongs to the gluconokinase gntK/gntV family and catalyzes the conversion of ATP and D-gluconate to ADP and 6-D-gluconate. Existing as three alternatively spliced isoforms, the gene encoding C9orf103 maps to human chromosome 9q21.32. Chromosome 9 consists of about 145 million bases, represents 4?% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Gene Full Name: IDNK gluconokinase
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Gene ID
- 414328
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UniProt
- Q5T6J7
Target
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