KLHL41 Antibody

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) KLHL41 Polyclonal antibody
Uniprot No.：

O60662
基因名：

KLHL41
別名：

cb52 antibody; fb24f05 antibody; fc15e07 antibody; Gm112 antibody; KBTBA_HUMAN antibody; Kbtbd10 antibody; Kel like protein 23 antibody; Kel-like protein 23 antibody; Kelch related protein 1 antibody; Kelch repeat and BTB domain-containing protein 10 antibody; Kelch-related protein 1 antibody; KRP1 antibody; MGC143407 antibody; Sarcosin antibody; sbcb52 antibody; wufb24f05 antibody; wufc15e07 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Kelch-like protein 41 protein (1-300AA)
免疫原種屬：

Homo sapiens (Human)

標(biāo)記方式：

Non-conjugated

本頁面中的產(chǎn)品，KLHL41 Antibody (CSB-PA011995LA01HU)，的標(biāo)記方式是Non-conjugated。對于KLHL41 Antibody，我們還提供其他標(biāo)記。見下表：

標(biāo)記方式	貨號	產(chǎn)品名稱	應(yīng)用
HRP	CSB-PA011995LB01HU	KLHL41 Antibody, HRP conjugated	ELISA
FITC	CSB-PA011995LC01HU	KLHL41 Antibody, FITC conjugated
Biotin	CSB-PA011995LD01HU	KLHL41 Antibody, Biotin conjugated	ELISA

克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

ELISA
Protocols：

ELISA Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

功能：

Involved in skeletal muscle development and differentiation. Regulates proliferation and differentiation of myoblasts and plays a role in myofibril assembly by promoting lateral fusion of adjacent thin fibrils into mature, wide myofibrils. Required for pseudopod elongation in transformed cells.
基因功能參考文獻(xiàn)：
1. Mutations in KLHL41 showed phenotype-genotype correlation: Frameshift mutations resulted in severe phenotypes with neonatal death, whereas missense changes resulted in impaired motor function with survival into late childhood and/or early adulthood. PMID: 24268659
相關(guān)疾病：

Nemaline myopathy 9 (NEM9)
亞細(xì)胞定位：

Cytoplasm. Cytoplasm, cytoskeleton. Cell projection, pseudopodium. Cell projection, ruffle. Cytoplasm, myofibril, sarcomere, M line. Sarcoplasmic reticulum membrane. Endoplasmic reticulum membrane.
組織特異性：

Sarcomeric muscle.
數(shù)據(jù)庫鏈接：

HGNC: 16905

OMIM: 607701

KEGG: hsa:10324

STRING: 9606.ENSP00000284669

UniGene: Hs.50550