Thermo Fisher Scientific Lamin A/C (R482W) Monoclonal Antibody (5H8-B4)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA518063 | - | Thermo Fisher Scientific MA518063 Lamin A/C (R482W) Monoclonal Antibody (5H8-B4) 100 ul pk | 재고문의 | pk | 785,000원 | - | 863,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:32,000
Immunocytochemistry (ICC/IF)
Assay-dependent
Immunoprecipitation (IP)
Assay-dependent
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
5H8-B4
Immunogen
Lamin A Ig-fold; human (Immunogen sequence: 430-545 (6xHis-tagged fusion protein)) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Lamin A/C (R482W),
uniProtId:
P02545-1,
ncbiNodeId:
9606,
antigenRange:
430-545,
antigenLength:
664,
antigenImageFileName:
MA5-18063_Lamin_AC_R482W_P02545-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-18063_Lamin_AC_R482W_P02545-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS
Contains
0.1% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2539446
Product Specific Information
This antibody recognizes the FPLD-associated lamin A/C mutant strain R482W.
Target Information
Lamins are a class of intermediate filament proteins that form a matrix on the inner surface of the nuclear envelope. These proteins are found in many different cell types in three different forms (A, B, and C). Lamins A and C are alternatively spliced versions of the LMNA gene. The LMNA gene has been linked to many disorders of the muscular system, nervous system, and the fat distributions systems including: Emery-Dreifuss muscular dystrophy, Dunnigan-type familial partial lipodystrophy (FPLD), limb-girdle muscular dystrophy (LGMD1B), dilated cardiomyopathy (CMD1A), axonal neuropathy (Charcot-Marie-Tooth disease; CMT2B1), and mandibuloacral dysplasia (MAD).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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