DDRGK1 antibody (AA 81-180)
Quick Overview for DDRGK1 antibody (AA 81-180) (ABIN1387986)
Target
See all DDRGK1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 81-180
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Predicted Reactivity
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human DDRGK1
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Isotype
- IgG
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Application Notes
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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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Storage
- 4 °C,-20 °C
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Storage Comment
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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Expiry Date
- 12 months
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- DDRGK1 (DDRGK Domain Containing 1 (DDRGK1))
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Alternative Name
- Ddrgk1
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Background
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Synonyms: Chromosome 20 open reading frame 116, DDRGK domain containing 1, DDRGK domain containing protein 1, DDRGK domain-containing protein 1, DDRGK_HUMAN, Ddrgk1, MGC2592, RGD1309979, RP23-100C5.9, dJ1187M17.3, 1110001I20Rik, 2600009E05Rik, C20orf116.
Background: DDRGK1 (DDRGK domain-containing protein 1), also known as C20orf116, is a 314 amino acid secreted protein. DDRGK1 contains one PCI domain and is expressed as two isoforms produced by alternative splicing. The gene that encodes DDRGK1 maps to human chromosome 20, which represents about 2 % of human DNA and consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought to be important for seminal production. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.
Target
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