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ELK Biotechnology CYB5R3 rabbit pAb
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ELK Biotechnology CYB5R3 rabbit pAb

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CYB5R3 rabbit pAb는 인간 CYB5R3 단백질을 표적으로 하는 고품질 폴리클로날 항체입니다. WB, IHC, IF, ELISA에 사용 가능하며, 다양한 종(Human, Rat, Mouse)에 반응합니다. 고농도(1 mg/ml)로 제공되어 안정적인 신호 검출이 가능합니다.

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pk
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ELK Biotechnology ES2077-100UL CYB5R3 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES2077-50UL CYB5R3 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology CYB5R3 rabbit pAb

ELK Biotechnology CYB5R3 rabbit pAb

제품 정보

항목 내용
Product name CYB5R3 rabbit pAb
Alternative Names CYB5R3; DIA1; NADH-cytochrome b5 reductase 3; B5R; Cytochrome b5 reductase; Diaphorase-1
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/40000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human CYB5R3 (AA range: 137-186)
Storage -20°C / 1 year
Host Rabbit
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 34 kD
GeneID (Human) 1727
Human Swiss-Prot No P00387
Cellular Localization Isoform 1: Endoplasmic reticulum membrane; Lipid-anchor; Cytoplasmic side. Mitochondrion outer membrane; Lipid-anchor; Cytoplasmic side.
Isoform 2: Cytoplasm. Produces the soluble form found in erythrocytes.
Species Reactivity Human; Rat; Mouse

Background

This gene encodes cytochrome b5 reductase, which includes a membrane-bound form in somatic cells (anchored in the endoplasmic reticulum, mitochondrial and other membranes) and a soluble form in erythrocytes.
The membrane-bound form exists mainly on the cytoplasmic side of the endoplasmic reticulum and functions in desaturation and elongation of fatty acids, in cholesterol biosynthesis, and in drug metabolism.
The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is involved in methemoglobin reduction.
The membrane-bound form has both membrane-binding and catalytic domains, while the soluble form has only the catalytic domain.
Alternate splicing results in multiple transcript variants. Mutations in this gene cause methemoglobinemias.
[provided by RefSeq, Jan 2010]

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