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Thermo Fisher Scientific ALDH3B2 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific ALDH3B2 Polyclonal Antibody, MaxPab

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Thermo Fisher Scientific의 ALDH3B2 폴리클로날 항체는 인간 ALDH3B2 단백질을 표적으로 하는 연구용 항체로, Western blot 등에서 사용 가능. Rabbit IgG 기반으로 제작되었으며, PBS 버퍼에 보존제 없이 액상 형태로 제공. 알코올 대사 관련 연구에 적합.

판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 10:59
Thermo Fisher Scientific H00000222-D01P ALDH3B2 Polyclonal Antibody, MaxPab 100 ug pk판매 단위 pk ·
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582,600원VAT 포함 640,860원

Thermo Fisher Scientific · Thermo Fisher Scientific ALDH3B2 Polyclonal Antibody, MaxPab

Applications

  • Western Blot (WB): Tested dilution 1–5 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen ALDH3B2 (AAH07685.1, 1–385 a.a.) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage buffer PBS, pH 7.4
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MKDEPRSTNL FMKLDSVFIW KEPFGLVLII APWNYPLNLT LVLLVGALAA GSCVVLKPSE ISQGTEKVLA EVLPQYLDQS CFAVVLGGPQ ETGQLLEHKL DYIFFTGSPR VGKIVMTAAT KHLTPVTLEL GGKNPCYVDD NCDPQTVANR VAWFCYFNAG QTCVAPDYVL CSPEMQERLL PALQSTITRF YGDDPQSSPN LGRIINQKQF QRLRALLGCG RVAIGGQSNE SDRYIAPTVL VDVQETEPVM QEEIFGPILP IVNVQSVDEA IKFINWQEKP LALYAFSNSS QVVNQMLERT SSGSFGGNEG FTYISLLSVP FGGVGHSGMG RYHGKFTFDT FSHHRTCLLA PSGLEKLKEI HYPPYTDWNQ QLLRWGMGSQ SCTLL


Target Information

ALDH3B2 (aldehyde dehydrogenase 3 family, member B2), also known as ALDH8, is a 385 amino acid protein that belongs to the ALDH family and is involved in alcohol metabolism. Expressed in salivary gland tissue, ALDH3B2 catalyzes the NADP⁺-dependent conversion of an aldehyde into an acid. The gene encoding ALDH3B2 maps to human chromosome 11, which contains over 1,400 genes and represents nearly 4% of the human genome. Mutations in genes located on chromosome 11 are associated with disorders such as Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.


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

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