ARG44500
anti-HDHD5 antibody
anti-HDHD5 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat
Overview
| Product Description | Rabbit Polyclonal antibody recognizes HDHD5 |
|---|---|
| Tested Reactivity | Hu, Ms, Rat |
| Tested Application | FACS, IHC-P, WB |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | HDHD5 |
| Antigen Species | Human |
| Immunogen | Human HDHD5 recombinant protein |
| Conjugation | Un-conjugated |
| Alternate Names | HDHD5; Haloacid Dehalogenase Like Hydrolase Domain Containing 5; CECR5; Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5; Cat Eye Syndrome Chromosome Region, Candidate 5; Cat Eye Syndrome Critical Region Protein 5 |
Application Instructions
| Application Suggestion |
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| Application Note | The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Affinity purified with Immunogen. |
| Buffer | 0.9% NaCl, 0.2% Na2HPO4, 0.05% Sodium azide and 4% Trehalose. |
| Preservative | 0.05% Sodium azide |
| Stabilizer | 4% Trehalose |
| Concentration | 0.5 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links |
Swiss-port # Q91WM2 Mouse Cat eye syndrome critical region protein 5 homolog Swiss-port # Q9BXW7 Human Cat eye syndrome critical region protein 5 |
|---|---|
| Gene Symbol | HDHD5 |
| Gene Full Name | Haloacid Dehalogenase Like Hydrolase Domain Containing 5 |
| Background | Predicted to be involved in glycerophospholipid biosynthetic process. Predicted to be active in mitochondrion. |
| Function | Candidate gene for the Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. Duplication usually takes in the form of a surpernumerary bisatellited isodicentric chromosome, resulting in four copies of the region (represents an inv dup22(q11)). CES is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. |
| Calculated MW | 46 kDa |
