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beta 2 Microglobulin (7D1)/HRP (bsm-41182M-HRP)  
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產品編號 bsm-41182M-HRP
英文名稱 beta 2 Microglobulin (7D1)/HRP
中文名稱 辣根過氧化物酶標記β2-微球蛋白單克隆抗體(檢測)
別    名 B2M; Beta-2-MG; Beta 2 microglobulin precursor; Beta chain of mhc class 1 proteins; Hdcma22p; B2MG_HUMAN; Beta 2 microglobin; Beta-2 microglobulin precursor; Beta chain of mhc class 1 proteins; Beta chain of MHC class I molecules; Beta-2-microglobulin form pI 5.3; CDABP0092.  β2 Microglobulin; β2-Microglobulin; β-2-Microglobulin; bsm-41168M
研究領域 免疫學  新陳代謝  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 7D1
交叉反應
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 13kDa
細胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Anti-beta 2 Microglobulin (7D1)/HRP 
亞    型 IgG
純化方法 affinity purified by Protein G
緩 沖 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 bsm-41168M(capture) is Matched Pair with bsm-41182M(detection).
This gene encodes a serum protein found in association with the major histocompatibility complex (MHC) class I heavy chain on the surface of nearly all nucleated cells. The protein has a predominantly beta-pleated sheet structure that can form amyloid fibrils in some pathological conditions. A mutation in this gene has been shown to result in hypercatabolic hypoproteinemia.[provided by RefSeq, Sep 2009].

Function:
Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.

Subunit:
Heterodimer of an alpha chain and a beta chain. Beta-2-microglobulin is the beta-chain of major histocompatibility complex class I molecules. Polymers of beta 2-microglobulin can be found in tissues from patients on long-term hemodialysis.

Subcellular Location:
Secreted. Note=Detected in serum and urine.

Post-translational modifications:
Glycation of Ile-21 is observed in long-term hemodialysis patients.

DISEASE:
Defects in B2M are the cause of hypercatabolic hypoproteinemia (HYCATHYP) [MIM:241600]. Affected individuals show marked reduction in serum concentrations of immunoglobulin and albumin, probably due to rapid degradation.
Note=Beta-2-microglobulin may adopt the fibrillar configuration of amyloid in certain pathologic states. The capacity to assemble into amyloid fibrils is concentration dependent. Persistently high beta(2)-microglobulin serum levels lead to amyloidosis in patients on long-term hemodialysis.

Similarity:
Belongs to the beta-2-microglobulin family.
Contains 1 Ig-like C1-type (immunoglobulin-like) domain.

SWISS:
P61769

Gene ID:
567

Database links:

Entrez Gene: 567 Human

Entrez Gene: 12010 Mouse

Entrez Gene: 24223 Rat

Omim: 109700 Human

SwissProt: P61769 Human

SwissProt: P01887 Mouse

SwissProt: P07151 Rat

Unigene: 534255 Human

Unigene: 702947 Human

Unigene: 163 Mouse

Unigene: 1868 Rat



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