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Thermo Fisher Scientific SHFM3 Polyclonal Antibody
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Thermo Fisher Scientific SHFM3 Polyclonal Antibody

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Human SHFM3 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB, IHC(P), ICC/IF 등 다양한 응용에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보존. 연구용으로만 사용.

카탈로그번호
PA560390
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 06:49
Thermo Fisher Scientific PA560390 SHFM3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SHFM3 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SHFM3. Recombinant protein control fragment (Product #RP-95598).
Conjugate Unconjugated
Form Liquid
Concentration 0.08 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, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2647272

Product Specific Information

Immunogen sequence:
QCLHTIQTED RVWSIAISPL LSSFVTGTAC CGHFSPLRIW DLNSGQLMTH LGSDFPPGAG VLDVMYESPF TLLSCGYD

Sequence identity:

  • Mouse: 97%
  • Rat: 95%

Target Information

This gene belongs to the F-box/WD-40 gene family, which recruits specific target proteins through WD-40 domains for ubiquitin-mediated degradation. In mouse, a similar protein maintains the apical ectodermal ridge during limb bud development. Disruption of the gene leads to absence of central digits and syndactyly, resembling human split hand-split foot malformation. This condition is genetically heterogeneous, with various inheritance modes. An autosomal recessive form maps to the same chromosomal region, and complex rearrangements involving duplications of this gene are associated with the disorder. A pseudogene is located within an intron of the BCR gene on chromosome 22.

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

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