Thermo Fisher Scientific SOX2 Monoclonal Antibody (GT1352)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA531456 | - | Thermo Fisher Scientific MA531456 SOX2 Monoclonal Antibody (GT1352) 100 ul pk | 재고문의 | pk | 660,000원 | - | 726,000원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:3,000
Immunohistochemistry (Paraffin) (IHC (P))
1:100-1:1,000
Immunohistochemistry (Frozen) (IHC (F))
1:100-1:1,000
Immunocytochemistry (ICC/IF)
1:100-1:1,000
Flow Cytometry (Flow)
1:50-1:200
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
GT1352
Immunogen
Recombinant protein encompassing a sequence within the center region of human SOX2.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS with 20% glycerol
Contains
no preservative
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_2787088
Product Specific Information
Keep as concentrated solution.
Predicted reactivity: Mouse (99%), Rat (99%), Zebrafish (92%), Japanese Medaka (88%), Xenopus laevis (90%), Cat (100%), Pig (98%), Chicken (94%), Sheep (100%), Rhesus Monkey (100%), Bovine (100%).
Positive Control: NT2D1, human ESC, mouse ESC.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
SOX2 is an intronless gene encoding a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of the SOX2 gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. The SOX2 gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). Further, SOX2 protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in the SOX2 gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation, optic nerve hypoplasia and syndromic microphthalmia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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