Thermo Fisher Scientific HOXD13 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA566661 | - | Thermo Fisher Scientific PA566661 HOXD13 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 794,000원 | - | 873,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
View 1 publication 1 publication
Product Specifications
Species Reactivity
Human
Published species
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant Human HOXD13. Recombinant protein control fragment (Product #RP-107309). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HOXD13,
uniProtId:
P35453-1,
ncbiNodeId:
9606,
antigenRange:
191-261,
antigenLength:
343,
antigenImageFileName:
PA5-66661_HOXD13_P35453-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-66661_HOXD13_P35453-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.1 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2662801
Product Specific Information
Immunogen sequence: SFYQGYTSPYQ HVPGYIDMVS TFGSGEPRHE AYISMEGYQS WTLANGWNSQ VYCTKDQPQG SHFWKSSFPG
Highest antigen sequence identity to the following orthologs - mouse 99%, rat 99%.
Target Information
HOXD13 (homeobox protein D13) belongs to a class of transcription factors called homeobox proteins. In vertebrates, homeobox are found in clusters called A, B, C, and D on four separate chromosomes. Expression of homeobox proteins is spatially and temporally regulated during embryonic development. The gene encoding HOXD13 is part of the D cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5` end of this cluster have been associated with severe limb and genital abnormalities. Mutations in the HOXD13 gene cause synpolydactyly.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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