GPR172B antibody (AA 210-290)
Quick Overview for GPR172B antibody (AA 210-290) (ABIN7223372)
Target
See all GPR172B AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 210-290
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Purpose
- GPR172B Polyclonal Antibody
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Specificity
- GPR172B Polyclonal Antibody detects endogenous levels of GPR172B protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the Internal region of human GPR172B at AA range: 210-290
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IF (1:200-1:1000), ELISA (1:10000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 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
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- GPR172B (G Protein-Coupled Receptor 172B (GPR172B))
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Alternative Name
- GPR172B
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Background
- Rabbit Anti-GPR172B Polyclonal Antibody,SLC52A1, GPR172B, PAR2, RFT1, Solute carrier family 52, riboflavin transporter, member 1, Porcine endogenous retrovirus A receptor 2, PERV-A receptor 2, Protein GPR172B, Riboflavin transporter 1, hRFT1,Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. SLC52A1 (solute carrier family 52 member 1) encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.,Solute carrier family 52 riboflavin transporter member 1
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Molecular Weight
- observerd band 46kDa
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Gene ID
- 55065
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UniProt
- Q9NWF4
Target
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