Thermo Fisher Scientific SMN1/SMN2 Monoclonal Antibody (2B1)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA15878 | - | Thermo Fisher Scientific MA15878 SMN1/SMN2 Monoclonal Antibody (2B1) 100 ul pk | 재고문의 | pk | 1,017,000원 | - | 1,118,700원 |
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Immunocytochemistry (ICC/IF)
Assay-dependent
Flow Cytometry (Flow)
Assay-dependent
ELISA (ELISA)
Assay-dependent
Immunoprecipitation (IP)
Assay-dependent
View 1 publication 1 publication
Product Specifications
Species Reactivity
Human, Mouse, Xenopus
Published species
Rabbit
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
2B1
Immunogen
Purified recombinant His 6 tagged-SMN protein.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein A
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_1087364
Product Specific Information
MA1-5878 detects SMN in human, mouse and xenopus samples.
MA1-5878 has been successfully used in Western blot, immunoprecipitation, immunofluorescence, immunohistochemistry (paraffin), flow cytometry, and ELISA procedures. MA1-5878 detects a band of approximately 42kDa.
The MA1-5878 immunogen is purified recombinant His 6 tagged-SMN protein (human).
Target Information
The SMN1 gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein - survival motor neuron protein. The SMN complex plays a catalyst role in the assemble of small nuclear ribonucleoproteins, the building blocks of the spliceosome. Mutations in the SMN1 gene are known to cause spinal muscular atrophy 1/2.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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