PRODH polyclonal antibody
产品名称： PRODH polyclonal antibody
英文名称： PRODH polyclonal antibody
产品编号： PAB6986
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Goat polyclonal antibody raised against synthetic peptide of PRODH.
- Immunogen:
- A synthetic peptide corresponding to internal region of human PRODH.
- Sequence:
- C-ERDGSGTNKRDKQYQ
- Host:
- Goat
- Theoretical MW (kDa):
- 68
- Reactivity:
- Human
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:16000)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (3-6 ug/mL)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Publication Reference
- 1.
- Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice.
Paterlini M, Zakharenko SS, Lai WS, Qin J, Zhang H, Mukai J, Westphal KG, Olivier B, Sulzer D, Pavlidis P, Siegelbaum SA, Karayiorgou M, Gogos JA.Nat Neurosci. 2005 Nov;8(11):1586-94. Epub 2005 Oct 23.
- Application Image
- Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
- enlarge
- ELISA
- Entrez GeneID:
- 5625
- Protein Accession#:
- NP_057419.2
- Gene Name:
- PRODH
- Gene Alias:
- FLJ33744,HSPOX2,MGC148078,MGC148079,PIG6,POX,PRODH1,PRODH2,SCZD4,TP53I6
- Gene Description:
- proline dehydrogenase (oxidase) 1
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome. [provided by RefSeq
- Other Designations:
- OTTHUMP00000196495,proline dehydrogenase 1,proline oxidase 2,proline oxidase, mitochondrial,tumor protein p53 inducible protein 6
- Gene Pathway
- Related Disease
- Amino Acid Metabolism, Inborn Errors
- Autistic Disorder
- Bipolar Disorder
- Cognition
- DiGeorge Syndrome
- DiGeorge syndrome
- Dominance, Cerebral
- Genetic Predisposition to Disease
- Memory
- Memory, Short-Term
- Mental Disorders
- Mental Retardation
- Psychotic Disorders
- Schizophrenia
- Schizophrenia
- Schizophrenic Psychology
- Schizotypal Personality Disorder
- Startle Reaction
- Verbal Learning