Thermo Fisher Scientific GluD1 Recombinant Rabbit Monoclonal Antibody (ARC1216)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 재고 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA535668 | - | Thermo Fisher Scientific MA535668 GluD1 Recombinant Rabbit Monoclonal Antibody (ARC1216) 100 ul pk | 재고문의 | pk | 612,000원 | - | 673,200원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000-1:4,000
Immunohistochemistry (Paraffin) (IHC (P))
1:200-1:2,000
Immunocytochemistry (ICC/IF)
1:50-1:200
ELISA (ELISA)
1 µg/mL
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Expression System
HEK293 cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
ARC1216
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 459-558 of human GLUD1 (P00367) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
GluD1,
uniProtId:
P00367-1,
ncbiNodeId:
9606,
antigenRange:
459-558,
antigenLength:
558,
antigenImageFileName:
MA5-35668_GluD1_P00367-1_Rabbit.svg,
antigenImageFileNamePDP:
MA5-35668_GluD1_P00367-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.51 mg/mL
Purification
Affinity Chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2849568
Product Specific Information
Immunogen sequence: ERDSNYHLLM SVQESLERKF GKHGGTIPIV PTAEFQDRIS GASEKDIVHS GLAYTMERSA RQIMRTAMKY NLGLDLRTAA YVNAIEKVFK VYNEAGVTFT
Target Information
Glutamate dehydrogenase, GluD1, is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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