IdnK antibody (AA 51-150) (HRP)
Quick Overview for IdnK antibody (AA 51-150) (HRP) (ABIN1711174)
Target
See all IdnK (IDNK) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 51-150
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Predicted Reactivity
- Human,Mouse
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human C9orf103
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Isotype
- IgG
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Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Handling Advice
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
- 12 months
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- IdnK (IDNK) (IdnK Gluconokinase Homolog (IDNK))
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Alternative Name
- C9orf103
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Background
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Synonyms: bA522I20.2, C9orf103, Chromosome 9 open reading frame 103, Glucokinase like protein, Gluconate kinase, Gluconokinase like protein, GNTK_HUMAN, IDNK, OTTHUMP00000021546, OTTHUMP00000021547, Probable gluconokinase, RP11-522I20.2.
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.
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Gene ID
- 414328
Target
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