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Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1063)
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Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1063)

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Human NSD2 단백질을 인식하는 CL1063 클론의 Mouse Monoclonal Antibody로, WB, IHC, ICC/IF에 적합합니다. Protein A로 정제된 액상형 항체이며, 1 mg/mL 농도. 연구용으로만 사용.

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pk
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마지막 업데이트 2025. 07. 28. 오후 03:39
Thermo Fisher Scientific MA524621 NSD2 Monoclonal Antibody (CL1063) 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific NSD2 Monoclonal Antibody (CL1063)

Applications

Application Tested Dilution Publications
Western Blot (WB) 1 µg/mL -
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:1,000 -
Immunocytochemistry (ICC/IF) 2–10 µg/mL View 1 publication

Product Specifications

Specification Description
Species Reactivity Human
Published Species Not Applicable
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone CL1063
Immunogen Recombinant protein corresponding to Human NSD2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
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_2637236

Product Specific Information

Immunogen sequence:
SANGKTPSCE VNRECSVFLS KAQLSSSLQE GVMQKFNGHD ALPFIPADKL KDLTSRVFNG EPGAHDAKLR FESQEMKGIG TPPNTTPIKN GSPEIKLKIT KTYMNGKPLF ESSICGD

Highest antigen sequence identity to orthologs:

  • Mouse: 91%
  • Rat: 91%

Binds to an epitope located within the peptide sequence ALPFIPADKL as determined by overlapping synthetic peptides.


Target Information

This gene encodes a protein containing four domains found in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously during early development.
Wolf-Hirschhorn syndrome (WHS) is associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and is also involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas.
Alternative splicing results in multiple transcript variants encoding different isoforms, with some being nonsense-mediated mRNA decay candidates.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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