Thermo Fisher Scientific HFE Recombinant Rabbit Monoclonal Antibody (2O7D2)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA542637 | - | Thermo Fisher Scientific MA542637 HFE Recombinant Rabbit Monoclonal Antibody (2O7D2) 100 ul pk | 재고문의 | pk | 786,000원 | - | 864,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:1,000
ELISA (ELISA)
1 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Expression System
HEK293 cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
2O7D2
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 249-348 of human HFE (Q30201). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HFE,
uniProtId:
Q30201-1,
ncbiNodeId:
9606,
antigenRange:
249-348,
antigenLength:
348,
antigenImageFileName:
MA5-42637_HFE_Q30201-1_Rabbit.svg,
antigenImageFileNamePDP:
MA5-42637_HFE_Q30201-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.6 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_2911778
Product Specific Information
Positive test controls include: HeLa, HT-29, A-549. The target is usually found in the following locations: Cell membrane, Single-pass type I membrane protein.
Immunogen sequence: KEFEPKDVLP NGDGTYQGWI TLAVPPGEEQ RYTCQVEHPG LDQPLIVIWE PSPSGTLVIG VISGIAVFVV ILFIGILFII LRKRQGSRGA MGHYVLAERE
Target Information
The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin. It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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